编号 |
Drug
药品名称 |
Drug Trade Name
药品商品名称 |
Approved Use
批准用途 |
Manufacturer
Distributor
制造商/销售商 |
Approval Date
批准日期 |
1 |
abarelix |
Plenaxis depot |
For the palliative treatment of men with advanced symptomatic prostate cancer, in whom LHRH agonist therapy is not appropriate and who refuse surgical castration, and have one or more of the following: (1) risk of neurological compromise due to metastases, (2) ureteral or bladder outlet obstruction due to local encroachment or metastatic disease, or (3) severe bone pain from skeletal metastases persisting on narcotic analgesia |
Praecis |
2003-11-25 |
2 |
aldesleukin |
Prokine |
Treatment of adults with metastatic melanoma |
Chiron |
1998-01-09 |
3 |
Aldesleukin |
Proleukin |
Treatment of adults with metastatic renal cell carcinoma |
Chiron Corp |
1992-05-05 |
4 |
Alemtuzumab |
Campath |
Accel. Approv. (clinical benefit not established) Campath is indicated for the treatment of B-cell chronic lymphocytic leukemia (B-CLL) in patients who have been treated with alkylating agents and who have failed fludarabine therapy. |
Millennium and ILEX Partners, LP |
2001-05-07 |
5 |
alitretinoin |
Panretin |
Topical treatment of cutaneous lesions in patients with AIDS-related Kaposi's sarcoma. |
Ligand Pharmaceuticals |
1999-02-02 |
6 |
allopurinol |
Zyloprim |
Patients with leukemia, lymphoma and solid tumor malignancies who are receiving cancer therapy which causes elevations of serum and urinary uric acid levels and who cannot tolerate oral therapy. |
GlaxoSmithKline |
1996-05-17 |
7 |
altretamine |
Hexalen |
Single agent palliative treatment of patients with persistent or recurrent ovarian cancer following first-line therapy with a cisplatin and/or alkylating agent based combination. |
US Bioscience |
1990-12-26 |
8 |
amifostine |
Ethyol |
To reduce the cumulative renal toxicity associated with repeated administration of cisplatin in patients with advanced ovarian cancer |
US Bioscience |
1995-12-08 |
9 |
amifostine |
Ethyol |
Accel. Approv. (clinical benefit not established) Reduction of platinum toxicity in non-small cell lung cancer |
US Bioscience |
1996-03-15 |
10 |
amifostine |
Ethyol |
To reduce post-radiation xerostomia for head and neck cancer where the radiation port includes a substantial portion of the parotid glands. |
US Bioscience |
1999-06-24 |
11 |
anakinra |
Kineret |
pediatric Use section of the US product label and to fulfill PMC #3 to assess the safety and efficacy of anakinra in pediatric patients with juvenile rheumatoid arthritis |
Amgen |
2006-12-15 |
12 |
anastrozole |
Arimidex |
Accel. Approv. (clinical benefit not established) for the adjuvant treatment of postmenopausal women with hormone receptor positive early breast cancer |
AstraZeneca |
2002-09-05 |
13 |
anastrozole |
Arimidex |
Conversion to regular approval for the adjuvant treatment of postmenopausal women with hormone receptor positive early breast cancer |
AstraZeneca |
2005-09-16 |
14 |
anastrozole |
Arimidex |
Treatment of advanced breast cancer in postmenopausal women with disease progression following tamoxifen therapy. |
AstraZeneca Pharmaceuticals |
1995-12-27 |
15 |
anastrozole |
Arimidex |
For first-line treatment of postmenopausal women with hormone receptor positive or hormone receptor unknown locally advanced or metastatic breast cancer. |
AstraZeneca Pharmaceuticals |
2000-09-01 |
16 |
arsenic trioxide |
Trisenox |
Second line treatment of relapsed or refractory APL following ATRA plus an anthracycline. |
Cell Therapeutic |
2000-09-25 |
17 |
asparaginase |
Elspar |
Therapy of patients with acute lymphocytic leukemia |
Merck |
1978-01-10 |
18 |
Asparaginase |
Elspar |
ELSPAR is indicated in the therapy of patients with acute lymphocytic leukemia. This agent is useful primarily in combination with other chemotherapeutic agents in the induction of remissions of the disease in pediatric patients. |
Merck & Co, Inc |
2002-08-01 |
19 |
azacitidine |
Vidaza |
For use for the treatment of patients with the following myelodysplastic syndrome subtypes: refractory anemia or refractory anemia with ringed sideroblasts (if accompanied by neutropenia or thrombocytopenia and requiring transfusions), refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, and chronic myelomonocytic leukemia |
Pharmion |
2004-05-19 |
20 |
azacitidine |
Vidaza |
indicated for treatment of patients with the following myelodysplastic syndrome subtypes: refractory anemia or refractory anemia with ringed sideroblasts (if accompanied by neutropenia or thrombocytopenia or requiring transfusions), refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, and chronic myelomonocytic leukemia. |
Pharmion |
2007-01-26 |
21 |
BCG Live |
TICE BCG |
|
Organon Teknika Corp |
1998-08-21 |
22 |
bevacizumab |
Avastin |
Metastatic colon carcinoma |
Genentech |
2006-06-20 |
23 |
bevacizumab |
Avastin |
FDA approved changed in the Avastin package insert regarding warning and dose and administration for Reversible Posterior Leukoencephalopathy Syndrome. Nasal septum perforation was also added as a serious adverse event. |
Genentech |
2006-09-21 |
24 |
bevacizumab |
Avastin |
a first-line treatment of patients with locally advanced, metastatic or recurrent non-small cell lung cancer in combination with platinum-based chemotherapy |
Genentech |
2006-10-11 |
25 |
bevacuzimab |
Avastin |
First-line treatment of patients with metastatic carcinoma of the colon and rectum (in combination with intravenous 5-fluorouracil-based chemotherapy) |
Genentech |
2004-02-26 |
26 |
bexarotene capsules |
Targretin |
For the treatment by oral capsule of cutaneous manifestations of cutaneous T-cell lymphoma in patients who are refractory to at least one prior systemic therapy. |
Ligand Pharmaceuticals |
1999-12-29 |
27 |
bexarotene gel |
Targretin |
For the topical treatment of cutaneous manifestations of cutaneous T-cell lymphoma in patients who are refractory to at least one prior systemic therapy. |
Ligand Pharmaceuticals |
2000-06-28 |
28 |
bleomycin |
Blenoxane |
|
Bristol-Myers Squibb |
1973-07-31 |
29 |
bleomycin |
Blenoxane |
Sclerosing agent for the treatment of malignant pleural effusion (MPE) and prevention of recurrent pleural effusions. |
Bristol-Myers Squibb |
1996-02-20 |
30 |
bortezombi |
Velcade |
for the treatment of patients with mantle cell lymphoma who have received at least one prior therapy |
Millennium |
2006-12-08 |
31 |
bortezomib |
Velcade |
Accel. Approv. (clinical benefit not established) for the treatment of multiple myeloma patients who have received at least two prior therapies and have demonstrated disease progression on the last therapy |
Millenium |
2003-05-13 |
32 |
bortezomib |
Velcade |
Conversion to regular approval for treatment of multiple myeloma patients who have received as least one prior therapy |
Millenium |
2005-03-25 |
33 |
busulfan intravenous |
Busulfex |
Use in combination with cyclophoshamide as conditioning regimen prior to allogeneic hematopoietic progenitor cell transplantation for chronic myelogenous leukemia. |
Orphan Medical, Inc |
1999-02-04 |
34 |
busulfan oral |
Myleran |
Chronic Myelogenous Leukemia- palliative therapy |
GlaxoSmithKline |
1954-06-26 |
35 |
calusterone |
Methosarb |
|
Pharmacia & Upjohn Company |
1973-02-20 |
36 |
capecitabine |
Xeloda |
Accel. Approv. (clinical benefit subsequently established) Treatment of metastatic breast cancer resistant to both paclitaxel and an anthracycline containing chemotherapy regimen or resistant to paclitaxel and for whom further anthracycline therapy may be contraindicated, e.g., patients who have received cumulative doses of 400 mg/m2 of doxorubicin or doxorubicin equivalents |
Roche |
1998-04-30 |
37 |
capecitabine |
Xeloda |
Initial therapy of patients with metastatic colorectal carcinoma when treatment with fluoropyrimidine therapy alone is preferred. Combination chemotherapy has shown a survival benefit compared to 5-FU/LV alone. A survival benefit over 5_FU/LV has not been demonstrated with Xeloda monotherapy. |
Roche |
2001-04-30 |
38 |
capecitabine |
Xeloda |
Conversion to regular approval for treatment in combination with docetaxel of patients with metastatic breast cancer after failure of prior anthracycline containing chemotherapy |
Roche |
2001-09-07 |
39 |
capecitabine |
Xeloda |
Adjuvant treatment in patients with Dukes’ C colon cancer who have undergone complete resection of the primary tumor when treatment with fluoropyrimidine therapy alone is preferred |
Roche |
2005-06-15 |
40 |
carboplatin |
Paraplatin |
Palliative treatment of patients with ovarian carcinoma recurrent after prior chemotherapy, including patients who have been previously treated with cisplatin. |
Bristol-Myers Squibb |
1989-03-03 |
41 |
carboplatin |
Paraplatin |
Initial chemotherapy of advanced ovarian carcinoma in combination with other approved chemotherapeutic agents. |
Bristol-Myers Squibb |
1991-07-05 |
42 |
carmustine |
BCNU, BiCNU |
|
Bristol-Myers Squibb |
1977-03-07 |
43 |
carmustine |
Gliadel |
Treatment of patients with malignant glioma undergoing primary surgical resection |
MGI Pharma |
2003-02-25 |
44 |
carmustine with Polifeprosan 20 Implant |
Gliadel Wafer |
For use in addition to surgery to prolong survival in patients with recurrent glioblastoma multiforme who qualify for surgery. |
Guilford Pharmaceuticals Inc. |
1996-09-23 |
45 |
celecoxib |
Celebrex |
Accel. Approv. (clinical benefit not established) Reduction of polyp number in patients with the rare genetic disorder of familial adenomatous polyposis. |
Searle |
1999-12-23 |
46 |
cetuximab |
Erbitux |
Accel. Approv. (clinical benefit not established) for treatment of EGFR-expressing metastatic colorectal carcinoma in patients who are refractory to irinotecan-based chemotherapy (in combination with irinotecan); as a single agent, treatment of EGFR-expressing metastatic colorectal carcinoma in patients who are intolerant to irinotecan-based chemotherapy |
Imclone |
2004-02-12 |
47 |
cetuximab |
Erbitux |
For use in combination with radiation therapy (RT) for the treatment of locally or regionally advanced squamous cell carcinoma of the head and neck (SCCHN) or as a single agent for the treatment of patients with recurrent or metastatic SCCHN for whom prior platinum-based therapy has failed. |
Imclone |
2006-03-01 |
48 |
chlorambucil |
Leukeran |
|
GlaxoSmithKline |
1957-03-08 |
49 |
cisplatin |
Platinol |
Metastatic testicular-in established combination therapy with other approved chemotherapeutic agents in patients with metastatic testicular tumors whoc have already received appropriate surgical and/or radiotherapeutic procedures. An established combination therapy consists of Platinol, Blenoxane and Velbam. |
Bristol-Myers Squibb |
1978-12-19 |
50 |
cisplatin |
Platinol |
Metastatic ovarian tumors - in established combination therapy with other approved chemotherapeutic agents: Ovarian-in established combination therapy with other approved chemotherapeutic agents in patients with metastatic ovarian tumors who have already received appropriate surgical and/or radiotherapeutic procedures. An established combination consists of Platinol and Adriamycin. Platinol, as a single agent, is indicated as secondary therapy in patients with metastatic ovarian tumors refractory to standard chemotherapy who have not previously received Platinol therapy. |
Bristol-Myers Squibb |
1978-12-19 |
51 |
cisplatin |
Platinol |
as a single agent for patients with transitional cell bladder cancer which is no longer amenable to local treatments such as surgery and/or radiotherapy. |
Bristol-Myers Squibb |
1993-04-22 |
52 |
cladribine |
Leustatin, 2-CdA |
Treatment of active hairy cell leukemia. |
R.W. Johnson Pharmaceutical Research Institute |
1993-02-26 |
53 |
clofarabine |
Clolar |
Accel. Approv. (clinical benefit not established) for the treatment of pediatric patients 1 to 21 years old with relapsed or refractory acute lymphoblastic leukemia after at least two prior regimens |
Genzyme |
2004-12-28 |
54 |
cyclophosphamide |
Cytoxan, Neosar |
|
Bristol-Myers Squibb |
1959-11-16 |
55 |
cyclophosphamide |
Cytoxan Injection |
|
Bristol-Myers Squibb |
1959-11-16 |
56 |
cyclophosphamide |
Cytoxan Injection |
|
Bristol-Myers Squibb |
1987-04-29 |
57 |
cyclophosphamide |
Cytoxan Tablet |
|
Bristol-Myers Squibb |
1987-04-29 |
58 |
cytarabine |
Cytosar-U |
|
Pharmacia & Upjohn Company |
1969-06-17 |
59 |
cytarabine liposomal |
DepoCyt |
Accel. Approv. (clinical benefit not established) Intrathecal therapy of lymphomatous meningitis |
Skye Pharmaceuticals |
1999-04-01 |
60 |
dacarbazine |
DTIC-Dome |
|
Bayer |
1975-05-27 |
61 |
dactinomycin, actinomycin D |
Cosmegen |
|
Merck |
1964-02-04 |
62 |
dactinomycin, actinomycin D |
dactinomycin, actinomycin D |
|
Merck |
1964-12-10 |
63 |
dalteparin sodium |
Fragmin |
provides for the use of Fragmin (dalteparin sodium injection) for extended treatment of symptomatic venous thromboembolism (VTE) [proximal deep vein thrombosis (DVT) and/or pulmonary embolism (PE)] to reduce the recurrence of VTE in patients with cancer. |
Pharmacia & Upjohn |
2007-05-01 |
64 |
darbepoetin alfa |
Aranesp |
for the treatment of anemia associated with chronic renal failure, including patients on dialysis and patients not on dialysis, and for the treatment of anemia in patients with non-myeloid malignancies where anemia is due to the effect of concomitantly administered chemotherapy. |
Amgen |
2007-03-09 |
65 |
darbepoetin alfa |
Aranesp |
|
Amgen |
2007-04-10 |
66 |
Darbepoetin alfa |
Aranesp |
Treatment of anemia associated with chronic renal failure. |
Amgen, Inc |
2001-09-17 |
67 |
Darbepoetin alfa |
Aranesp |
Aranesp is indicated for the treatment of anemia in patients with non- myeloid malignancies where anemia is due to the effect of concomitantly administered chemotherapy. |
Amgen, Inc |
2002-07-19 |
68 |
dasatinib |
Sprycel |
Chronic myelogenous leukemia |
Bristol Myers Squibb |
2006-06-28 |
69 |
daunorubicin liposomal |
DanuoXome |
First line cytotoxic therapy for advanced, HIV related Kaposi's sarcoma. |
Nexstar, Inc. |
1996-04-08 |
70 |
daunorubicin, daunomycin |
Daunorubicin |
Leukemia/myelogenous/monocytic/erythroid of adults/remission induction in acute lymphocytic leukemia of children and adults. |
Bedford Labs |
1998-01-30 |
71 |
daunorubicin, daunomycin |
Cerubidine |
In combination with approved anticancer drugs for induction of remission in adult ALL. |
Wyeth Ayerst |
1987-03-11 |
72 |
decitabine |
Dacogen |
for the treatment of patients with myelodysplastic syndromes (MDS) including previously treated and untreated, de novo and secondary MDS of all French-American-British subtypes (refractory anemia, refractory anemia with ringed sideroblasts, refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, and chronic myelomonocytic leukemia) and intermediate-1, intermediate-2, and high-risk International Prognostic Scoring System groups. |
MGI PHARMA INC |
2006-05-05 |
73 |
denileukin |
Ontak |
|
Seragen |
0000-00-00 |
74 |
Denileukin diftitox |
Ontak |
Accel. Approv. (clinical benefit not established) treatment of patients with persistent or recurrent cutaneous T-cell lymphoma whose malignant cells express the CD25 component of the IL-2 receptor |
Seragen, Inc |
1999-02-05 |
75 |
dexrazoxane |
Zinecard |
Accel. Approv. (clinical benefit subsequently established) Prevention of cardiomyopathy associated with doxorubicin administration |
Pharmacia & Upjohn Company |
1995-05-26 |
76 |
dexrazoxane |
Zinecard |
Conversion to regular approval for reducing the incidence and severity of cardiomyopathy associated with doxorubicin administration in women with metastatic breast cancer who have received a cumulative doxorubicin dose of 300 mg/m2 and who will continue to receive doxorubicin therapy to maintain tumor control. It is not recommended for use with the initiation of doxorubicin therapy. |
Pharmacia & Upjohn Company |
2002-10-31 |
77 |
docetaxel |
Taxotere |
Accel. Approv. (clinical benefit subsequently established) Treatment of patients with locally advanced or metastatic breast cancer who have progressed during anthracycline-based therapy or have relapsed during anthracycline-based adjuvant therapy. |
Aventis Pharmaceutical |
1996-05-14 |
78 |
docetaxel |
docetaxel |
Conversion to regular approval - treatment of locally advanced or metastatic breast cancer which has progressed during anthracycline-based treatment or relapsed during anthracycline-based adjuvant therapy |
Aventis Pharmaceutical |
1998-06-22 |
79 |
docetaxel |
Taxotere |
For locally advanced or metastatic non-small cell lung cancer after failure of prior platinum-based chemotherapy. |
Aventis Pharmaceutical |
1999-12-23 |
80 |
docetaxel |
Taxotere |
for use in combination with cisplatin for the treatment of patients with unresectable, locally advanced or metastatic non-small cell lung cancer who have not previously received chemotherapy for this condition cisplatin for the treatment of patients with unresectable, locally advanced or metastatic non-small cell lung cancer who have not previously received chemotherapy for this condition. |
Aventis Pharmaceutical |
2002-11-27 |
81 |
docetaxel |
Taxotere |
For use in combination with prednisone as a treatment for patients with androgen independent (hormone refractory) metastatic prostate cancer |
Aventis Pharmaceutical |
2004-05-19 |
82 |
docetaxel |
Taxotere |
For use in combination with doxorubicin and cyclophosphamide for the adjuvant treatment of patients with operable nodepositive breast cancer |
Aventis Pharmaceutical |
2004-08-18 |
83 |
docetaxel |
Taxotere |
for use in combination with cisplatin and fluorouracil for the induction treatment of patients with inoperable, locally advanced squamous cell carcinoma of the head and neck. |
Sanofi Aventis |
2006-10-17 |
84 |
doxorubicin |
Adriamycin PFS |
For use in combination with cyclophosphamide as a component of adjuvant therapy in patients with evidence of axillary node tumor involvement following resection of primary breast |
cancer Pharmacia |
2003-05-08 |
85 |
doxorubicin |
Adriamycin, Rubex |
|
Pharmacia & Upjohn Company |
1974-08-07 |
86 |
doxorubicin |
Adriamycin PFS Injectionintravenous injection |
Antibiotic, antitumor agent. |
Pharmacia & Upjohn Company |
1987-12-23 |
87 |
doxorubicin liposomal |
Doxil |
Conversion to regular approval for treatment of patients with ovarian cancer whose disease has progressed or recurred after platinum-based chemotherapy |
Alza |
2005-01-28 |
88 |
doxorubicin liposomal |
Doxil |
Accel. Approv. (clinical benefit not established) Treatment of AIDS-related Kaposi's sarcoma in patients with disease that has progressed on prior combination chemotherapy or in patients who are intolerant to such therapy. |
Sequus Pharmaceuticals, Inc. |
1995-11-17 |
89 |
doxorubicin liposomal |
Doxil |
Accel. Approv. (clinical benefit not established) Treatment of metastatic carcinoma of the ovary in patient with disease that is refractory to both paclitaxel and platinum based regimens |
Sequus Pharmaceuticals, Inc. |
1999-06-28 |
90 |
DROMOSTANOLONE PROPIONATE |
DROMOSTANOLONE |
|
Eli Lilly |
1961-10-26 |
91 |
DROMOSTANOLONE PROPIONATE |
MASTERONE INJECTION |
|
SYNTEX |
1964-10-08 |
92 |
eculizumab |
Soliris |
for the treatment of paroxysmal nocturnal hemoglobinuria (PNH) to reduce hemolysis. |
Alexion |
2007-03-16 |
93 |
Elliott's B Solution |
Elliott's B Solution |
Diluent for the intrathecal administration of methotrexate sodium and cytarabine for the prevention or treatment of meningeal leukemia or lymphocytic lymphoma. |
Orphan Medical, Inc |
1996-09-27 |
94 |
epirubicin |
Ellence |
A component of adjuvant therapy in patients with evidence of axillary node tumor involvement following resection of primary breast cancer. |
Pharmacia & Upjohn Company |
1999-09-15 |
95 |
epirubicin hcl |
epirubicin hcl |
as a component of adjuvant therapy in patients with evidence of axillary node tumor involvement following resection of primary breast cancer. |
Mayne |
2006-09-15 |
96 |
epoetin alfa |
Epogen/Procrit |
is indicated for the treatment of anemia related to therapy with zidovudine in HIV-infected patients. EPOGEN® is indicated to elevate or maintain the red blood cell level (as manifested by the hematocrit or hemoglobin determinations) and to decrease the need for transfusions in these patients. EPOGEN® is not indicated for the treatment of anemia in HIV-infected patients due to other factors such as iron or folate deficiencies, hemolysis, or gastrointestinal bleeding, which should be managed appropriately. |
Amgen |
2007-03-09 |
97 |
Epoetin alfa |
epogen |
EPOGENB is indicated for the treatment of anemia in patients with non-myeloid malignancies where anemia is due to the effect of concomitantly administered chemotherapy. EPOGEND is indicated to decrease the need for transfusions in patients who will be receiving concomitant chemotherapy for a minimum of 2 months. EPOGENB is not indicated for the treatment of anemia in cancer patients due to other factors such as iron or folate deficiencies, hemolysis or gastrointestinal bleeding, which should be managed appropriately. |
Amgen, Inc |
1999-07-26 |
98 |
Epoetin alfa |
epogen |
EPOGENB is indicated for the reatment of anemia related to therapy with zidovudine in HIV- infected patients. EPOGENB is indicated to elevate or maintain the red blood cell level (as manifested by the hematocrit or hemoglobin determinations) and to decrease the need for transfusions in these patients. EPOGEND is not indicated for the treatment of anemia in HIV-infected patients due to other factors such as iron or folate deficiencies, hemolysis or gastrointestinal bleeding, which should be managed appropriately. |
Amgen, Inc |
1999-07-26 |
99 |
Epoetin alfa |
epogen |
EPOGENB is indicated for the treatment of anemic patients (hemoglobin > 10 to _< 13 g/dL) scheduled to undergo elective, noncardiac, nonvascular surgery to reduce the need for allogeneic blood transfusions. |
Amgen, Inc |
1999-07-26 |
100 |
Epoetin alfa |
epogen |
EPOGEN is indicated for the treatment of anemia associated with CRF, including patients on dialysis (ESRD) and patients not on dialysis. |
Amgen, Inch |
1999-07-26 |
101 |
erlotinib |
Tarceva |
For treatment of locally advanced or metastatic Non Small-Cell Lung Cancer (NSCLC) after failure of at least one prior chemotherapy regimen |
OSI |
2004-11-18 |
102 |
erlotinib |
Tarceva |
For use in combination with gemcitabine for the first-line treatment of patients with locally advanced, unresectable or metastatic pancreatic cancer |
OSI |
2005-11-02 |
103 |
estramustine |
Emcyt |
palliation of prostate cancer |
Pharmacia & Upjohn Company |
1981-12-24 |
104 |
etoposide phosphate |
Etopophos |
Management of refractory testicular tumors, in combination with other approved chemotherapeutic agents. |
Bristol-Myers Squibb |
1996-05-17 |
105 |
etoposide phosphate |
Etopophos |
Management of small cell lung cancer, first-line, in combination with other approved chemotherapeutic agents. |
Bristol-Myers Squibb |
1996-05-17 |
106 |
etoposide phosphate |
Etopophos |
anagement of refractory testicular tumors and small cell lung cancer. |
Bristol-Myers Squibb |
1998-02-27 |
107 |
etoposide, VP-16 |
Vepesid |
efractory testicular tumors-in combination therapy with other approved chemotherapeutic agents in patients with refractory testicular tumors who have already received appropriate surgical, chemotherapeutic and radiotherapeutic therapy. |
Bristol-Myers Squibb |
1983-11-10 |
108 |
etoposide, VP-16 |
VePesid |
In combination with other approved chemotherapeutic agents as first line treatment in patients with small cell lung cancer. |
Bristol-Myers Squibb |
1986-12-30 |
109 |
etoposide, VP-16 |
Vepesid |
In combination with other approved chemotherapeutic agents as first line treatment in patients with small cell lung cancer. |
Bristol-Myers Squibb |
1986-12-30 |
110 |
exemestane |
Aromasin |
For adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer who have received two to three years of tamoxifen and are switched to AROMASIN® for completion of a total of five consecutive years of adjuvant hormonal therapy |
Pharmacia |
2005-10-05 |
111 |
exemestane |
Aromasin |
Treatment of advance breast cancer in postmenopausal women whose disease has progressed following tamoxifen therapy. |
Pharmacia & Upjohn Company |
1999-10-21 |
112 |
fentanyl citrate |
Fentora |
for the management of breakthrough pain in patients with cancer who are already receiving and who are tolerant to opioid therapy for their underlying persistent cancer pain. |
Cephalon |
2006-09-25 |
113 |
Filgrastim |
Neupogen |
Decrease incidence of infection in patients with nonmyeloid malignancies |
Amgen, Inc |
1991-02-20 |
114 |
Filgrastim |
Neupogen |
NEUPOGEN is indicated to decrease the incidence of infection‚ as manifested by febrile neutropenia‚ in patients with nonmyeloid malignancies receiving myelosuppressive anticancer drugs associated with a significant incidence of severe neutropenia with fever. |
Amgen, Inc |
1998-04-02 |
115 |
Filgrastim |
Neupogen |
NEUPOGEN is indicated for reducing the time to neutrophil recovery and the duration of fever, following induction or consolidation hemotherapy treatment of adults with AML. |
Amgen, Inc |
1998-04-02 |
116 |
Filgrastim |
Neupogen |
NEUPOGEN is indicated to reduce the duration of neutropenia and neutropenia-related clinical sequelae, eg, febrile neutropenia, in patients with nonmyeloid malignancies undergoing myeloablative chemotherapy followed by marrow transplantation. |
Amgen, Inc |
1998-04-02 |
117 |
floxuridine (intraarterial) |
FUDR |
|
Roche |
1970-12-08 |
118 |
fludarabine |
Fludara |
Palliative treatment of patients with B-cell lymphocytic leukemia (CLL) who have not responded or have progressed during treatment with at least one standard alkylating agent containing regimen. |
Berlex Laboratories Inc. |
1991-04-18 |
119 |
fluorouracil, 5-FU |
Adrucil |
prolong survival in combination with leucovorin |
ICN Puerto Rico |
1962-04-25 |
120 |
fulvestrant |
Faslodex |
the treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following antiestrogen therapy |
IPR |
2002-04-25 |
121 |
gefitinib |
Iressa |
Accel. Approv. (clinical benefit not established ) as monotherapy for the treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of both platinum-based and docetaxel chemotherapies |
AstraZenca |
2003-05-05 |
122 |
gemcitabine |
Gemzar |
Treatment of patients with locally advanced (nonresectable stage II or III) or metastatic (stage IV) adenocarcinoma of the pancreas. Indicated for first-line treatment and for patients previously treated with a 5-fluorouracil-containing regimen. |
Eli Lilly |
1996-05-15 |
123 |
gemcitabine |
Gemzar |
For use in combination with cisplatin for the first-line treatment of patients with inoperable, locally advanced (Stage IIIA or IIIB) or metastatic (Stage IV) non-small cell lung cancer. |
Eli Lilly |
1998-08-25 |
124 |
gemcitabine hcl |
Gemzar |
Ovarian cancer |
Lilly |
2006-07-14 |
125 |
gemicitabine |
Gemzar |
For use in combination with paclitaxel for the first-line treatment of patients with metastatic breast cancer after failure of prior anthracycline-containing adjuvant chemotherapy, unless anthracyclines were clinically contraindicated |
Lilly |
2004-05-19 |
126 |
gemtuzumab ozogamicin |
Mylotarg |
Accel. Approv. (clinical benefit not established) Treatment of CD33 positive acute myeloid leukemia in patients in first relapse who are 60 years of age or older and who are not considered candidates for cytotoxic chemotherapy. |
Wyeth Ayerst |
2000-05-17 |
127 |
goserelin acetate |
Zoladex |
|
AstraZeneca Pharmaceuticals |
1995-12-18 |
128 |
goserelin acetate |
Zoladex Implant |
Palliative treatment of advanced breast cancer in pre- and perimenopausal women. |
AstraZeneca Pharmaceuticals |
1995-12-18 |
129 |
histrelin acetate |
Histrelin implant |
For the palliative treatment of advanced prostate cancer |
Valera |
2004-10-12 |
130 |
hydroxyurea |
Hydrea |
|
Bristol-Myers Squibb |
1967-12-07 |
131 |
hydroxyurea |
Hydrea |
Decrease need for transfusions in sickle cell anemia |
Bristol-Myers Squibb |
1998-02-25 |
132 |
Ibritumomab Tiuxetan |
Zevalin |
Accel. Approv. (clinical benefit not established) treatment of patients with relapsed or refractory low-grade, follicular, or transformed B-cell non-Hodgkin's lymphoma, including patients with Rituximab refractory follicular non-Hodgkin’s lymphoma. |
IDEC Pharmaceuticals Corp |
2002-02-19 |
133 |
idarubicin |
Idamycin |
For use in combination with other approved antileukemic drugs for the treatment of acute myeloid leukemia (AML) in adults. |
Adria Laboratories |
1990-09-27 |
134 |
idarubicin |
Idamycin |
In combination with other approved antileukemic drugs for the treatment of acute non-lymphocytic leukemia in adults. |
Pharmacia & Upjohn Company |
1997-02-17 |
135 |
ifosfamide |
IFEX |
Third line chemotherapy of germ cell testicular cancer when used in combination with certain other approved antineoplastic agents. |
Bristol-Myers Squibb |
1988-12-30 |
136 |
imatinib mesylate |
Gleevec |
Accel. Approv. (clinical benefit not established) Initial therapy of chronic myelogenous leukemia |
Novartis |
2001-05-10 |
137 |
imatinib mesylate |
Gleevec |
Accel. Approv. (clinical benefit not established) metastatic or unresectable malignant gastrointestinal stromal tumors |
Novartis |
2002-02-01 |
138 |
Imatinib mesylate |
Gleevec |
Accel. Approv. (clinical benefit not established) Treatment of patients with Kit (CD117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumors (GIST). |
Novartis |
2002-02-01 |
139 |
imatinib mesylate |
Gleevec |
Accel. Approv. (clinical benefit not established) Initial treatment of newly diagnosed Ph+ chronic myelogenous leukemia (CML). |
Novartis |
2002-12-20 |
140 |
imatinib mesylate |
Gleevec |
Accel. Approv. (clinical benefit not established) for treatment of newly diagnosed adult patients with Philadelphia chromosome positive chronic myeloid leukemia (CML) in chronic phase. Follow-up is limited. Gleevec is also indicated for the treatment of patients with Philadelphia chromosome positive chronic myeloid leukemia (CML) in blast crisis, accelerated phase, or in chronic phase after failure of interferon-alpha therapy. There are no controlled trials demonstrating a clinical benefit, such as improvement in disease-related symptoms or increased survival in patients with CML blast crisis, accelerated phase or chronic phase after failure of alpha interferon. Gleevec is also indicated for the treatment of patients with Kit (CD117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumors (GIST) |
Novartis |
2003-04-18 |
141 |
imatinib mesylate |
Gleevec |
Accel. Approv. (clinical benefit not established) Treatment of pediatric patients with Ph+ chronic phase CML whose disease has recurred after stem cell transplant or who are resistant to interferon alpha therapy. |
Novartis |
2003-05-20 |
142 |
imatinib mesylate |
Gleevec |
Conversion to regular approval for treatment of patients with Philadelphia chromosome positive chronic myeloid leukemia (CML) in blast crisis, accelerated phase, or in chronic phase after failure of interferon-alpha therapy |
Novartis |
2003-12-08 |
143 |
imatinib mesylate |
Gleevec |
for the treatment of pediatric patients with newly diagnosed Philadelphia chromosome positive chronic myelogenous leukemia (Ph+ CML). |
Novartis |
2006-09-27 |
144 |
imatinib mesylate |
Gleevec |
single agent for the treatment of multiple indications |
Novartis |
2006-10-19 |
145 |
interferon alfa 2a |
Roferon A |
Treatment of patients with hairy cell leukemia |
Roche |
1986-06-04 |
146 |
interferon alfa 2a |
Roferon A |
Chronic phase, Philadelphia chromosome positive chronic myelogenous leukemia (CML) patients who are minimally pretreated (within 1 year of diagnosis) |
Roche |
1995-10-19 |
147 |
Interferon alfa-2a |
Roferon-A |
|
Hoffmann-La Roche Inc |
1996-11-01 |
148 |
Interferon alfa-2b |
Intron A |
Interferon alfa-2b, recombinant for Injection is indicated for the treatment of patients 18 years of age or older with hairy cell leukemia. |
Schering Corp |
1986-06-04 |
149 |
Interferon alfa-2b |
Intron A |
Interferon alfa-2b, recombinant for Injection is indicated for intralesional treatment of selected patients 18 years of age or older with condylomata acuminata involving external surfaces of the genital and perianal areas. |
Schering Corp |
1988-06-06 |
150 |
Interferon alfa-2b |
Intron A |
Interferon alfa-2b, recombinant for injection is indicated for the treatment of selected patients 18 years of age or older with AIDS-related Kaposi's Sarcoma. The likelihood of response to INTRON A therapy is greater in patients who are without systemic symptoms, who have limited lymphadenopathy and who have a relatively intact immune system as indicated by total CD4 count. |
Schering Corp |
1988-11-21 |
151 |
Interferon alfa-2b |
Intron A |
Interferon alfa-2b, recombinant for injection is indicated as adjuvant to surgical treatment in patients 18 years of age or older with malignant melanoma who are free of disease but at high risk for systemic recurrence within 56 days of surgery. |
Schering Corp |
1995-12-05 |
152 |
Interferon alfa-2b |
Intron A |
Interferon alfa-2b, recombinant for Injection is indicated for the initial treatment of clinically aggressive follicular non-Hodgkin’s Lymphoma in conjunction with anthracycline-containing combination chemotherapy in patients 18 years of age or older. |
Schering Corp |
1997-11-06 |
153 |
Interferon alfa-2b |
Intron A Intron A |
|
Schering Corp |
2002-06-21 |
154 |
irinotecan |
Camptosar |
Accel. Approv. (clinical benefit subsequently established) Treatment of patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following 5-FU-based therapy. |
Pharmacia & Upjohn Company |
1996-06-14 |
155 |
irinotecan |
Camptosar |
Conversion to regular approval - treatment of metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following 5-FU-based therapy. |
Pharmacia & Upjohn Company |
1998-10-22 |
156 |
irinotecan |
Camptosar |
For first line treatment n combination with 5-FU/leucovorin of metastatic carcinoma of the colon or rectum. |
Pharmacia & Upjohn Company |
2000-04-20 |
157 |
lapatinib ditosylate |
Tykerb |
for use in combination with capecitabine for the treatment of patients with advanced or metastatic breast cancer whose tumors overexpress HER2 (ErbB2) and who have received prior therapy including an anthracycline, a taxane, and trastuzumab. |
SmithKline Beecham |
2007-03-13 |
158 |
lapatinib ditosylate |
Tykerb |
|
mithKline Beecham |
2007-04-27 |
159 |
lenalidomide |
Revlimid |
Multiple myeloma |
Celegene |
2006-06-29 |
160 |
lenalidomide |
Revlimid |
for the treatment of patients with transfusion-dependent anemia due to Low- or Intermediate-1-risk myelodysplastic syndromes associated with a deletion 5q cytogenetic abnormality with or without additional cytogenetic abnormalities |
Celgene |
2005-12-27 |
161 |
letrozole |
Femara |
Treatment of advanced breast cancer in postmenopausal women. |
Novartis |
1997-07-25 |
162 |
letrozole |
Femara |
First-line treatment of postmenopausal women with hormone receptor positive or hormone receptor unknown locally advanced or metastatic breast cancer. |
Novartis |
2001-01-10 |
163 |
letrozole |
Femara |
|
Novartis |
2003-01-17 |
164 |
letrozole |
Femara |
Accel. Approv. (clinical benefit not established) for the extended adjuvant treatment of early breast cancer in postmenopausal women who have received five years of adjuvant tamoxifen therapy. |
Novartis |
2004-10-29 |
165 |
leucovorin |
Wellcovorin, Leucovorin |
Leucovorin calcium is indicated fro use in combination with 5-fluorouracil to prolong survival in the palliative treatment of patients with advanced colorectal cancer. |
Immunex Corporation |
1952-06-20 |
166 |
leucovorin |
Leucovorin |
|
Immunex Corporation |
1987-01-30 |
167 |
leucovorin |
Leucovorin |
|
Immunex Corporation |
1987-01-30 |
168 |
leucovorin |
Leucovorin |
|
Immunex Corporation |
1988-08-31 |
169 |
leucovorin |
Leucovorin |
n combination with fluorouracil to prolong survival in the palliative treatment of patients with advanced colorectal cancer. |
Lederle Laboratories |
1991-12-12 |
170 |
Leuprolide Acetate |
Eligard |
palliative treatment of advanced prostate cancer. |
QLT USA |
2002-01-23 |
171 |
levamisole |
Ergamisol |
Adjuvant treatment in combination with 5-fluorouracil after surgical resection in patients with Dukes' Stage C colon cancer. |
Janssen Research Foundation |
1990-06-18 |
172 |
lomustine, CCNU |
CeeBU |
|
Bristol-Myers Squibb |
1976-08-04 |
173 |
meclorethamine, nitrogen mustard |
Mustargen |
|
Merck |
1949-03-15 |
174 |
megestrol acetate |
Megace |
|
Bristol-Myers Squibb |
1971-08-18 |
175 |
melphalan, L-PAM |
Alkeran |
|
GlaxoSmithKline |
1964-01-17 |
176 |
melphalan, L-PAM |
Alkeran |
Systemic administration for palliative treatment of patients with multiple myeloma for whom oral therapy is not appropriate. |
GlaxoSmithKline |
1992-11-18 |
177 |
mercaptopurine, 6-MP |
Purinethol |
|
GlaxoSmithKline |
1953-09-11 |
178 |
mesna |
Mesnex |
Prevention of ifosfamide-induced hemorrhagic cystitis |
Asta Medica |
1988-12-30 |
179 |
mesna |
Mesnex tabs |
Reducing the incidence of ifosfamide-induced hemorrhagic cystitis |
Baxter |
2002-03-21 |
180 |
methotrexate |
Methotrexate |
|
Lederle Laboratories |
1953-12-07 |
181 |
methotrexate |
Methotrexate |
|
Lederle Laboratories |
1959-08-10 |
182 |
methotrexate |
Methotrexate |
|
Lederle Laboratories |
1971-11-01 |
183 |
methotrexate |
Methotrexate |
|
Lederle Laboratories |
1971-11-01 |
184 |
methotrexate |
Methotrexate |
osteosarcoma |
Lederle Laboratories |
1988-04-07 |
185 |
methotrexate |
Methotrexate |
|
Lederle Laboratories |
1988-10-31 |
186 |
methoxsalen |
Uvadex |
For the use of UVADEX with the UVAR Photopheresis System in the palliative treatment of the skin manifestations of cutaneous T-cell lymphoma (CTCL) that is unresponsive to other forms of treatment. |
Therakos |
1919-02-25 |
187 |
mitomycin C |
Mutamycin |
|
Bristol-Myers Squibb |
1974-05-28 |
188 |
mitomycin C |
Mitozytrex |
therapy of disseminated adenocarcinoma of the stomach or pancreas in proven combinations with other approved chemotherapeutic agents and as palliative treatment when other modalities have failed. |
Supergen |
2002-11-14 |
189 |
mitotane |
Lysodren |
|
Bristol-Myers Squibb |
1970-07-08 |
190 |
mitoxantrone |
Novantrone |
For use in combination with corticosteroids as initial chemotherapy for the treatment of patients with pain related to advanced hormone-refractory prostate cancer. |
Immunex Corporation |
1996-11-13 |
191 |
mitoxantrone |
Novantrone |
For use with other approved drugs in the initial therapy for acute nonlymphocytic leukemia (ANLL) in adults. |
Lederle Laboratories |
1987-12-23 |
192 |
nandrolone phenpropionate |
Durabolin-50 |
|
Organon |
1959-10-30 |
193 |
nelarabine |
Arranon |
Accel. Approv. (clinical benefit not established) for the treatment of patients with T-cell acute lymphoblastic leukemia and T-cell lymphoblastic lymphoma whose disease has not responded to or has relapsed following treatment with at least two chemotherapy regimens |
GlaxoSmithKline |
2005-10-28 |
194 |
Nofetumomab |
Verluma |
|
Boehringer Ingelheim Pharma KG (formerly Dr. Karl Thomae GmbH) |
1996-08-20 |
195 |
Oprelvekin |
Neumega |
Prevention of severe thrombocytopenia following myelosuppressive chemotherapy |
Genetics Institute, Inc |
1997-11-25 |
196 |
Oprelvekin |
Neumega |
|
Genetics Institute, Inc |
2002-09-18 |
197 |
Oprelvekin |
Neumega |
Neumega is indicated for the prevention of severe thrombocytopenia and the reduction of the need for platelet transfusions following myelosuppressive chemotherapy in adult patients with nonmyeloid malignancies who are at high risk of severe thrombocytopenia. |
Genetics Institute, Inc |
2002-09-18 |
198 |
oprelvekin |
Neumega |
warnings regarding ophthalmologic and ventricular arrhythmias adverse events have been added to the oprelvekin (Neumega) label |
Wyeth |
2006-09-13 |
199 |
oxaliplatin |
Eloxatin |
Accel. Approv. (clinical benefit not established) in combination with infusional 5-FU/LV, is indicated for the treatment of patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed during or within 6 months of completion of first line therapy with the combination of bolus 5-FU/LV and irinotecan. |
Sanofi Synthelabo |
2002-08-09 |
200 |
oxaliplatin |
Eloxatin |
Conversion to regular approval for use in combination with infusional 5-Fluorouracil (5-FU) and Leucovorin (LV) for the treatment of patients previously untreated for advanced colorectal cancer |
Sanofi Synthelabo |
2004-01-09 |
201 |
oxaliplatin |
Eloxatin |
for use in combination with infusional 5-FU/LV, for the adjuvant treatment of stage III colon cancer patients who have undergone complete resection of the primary tumor |
Sanofi Synthelabo |
2004-11-04 |
202 |
paclitaxel |
Abraxane |
for the treatment of breast cancer after failure of combination chemotherapy for metastatic disease or relapse within 6 months of adjuvant chemotherapy. Prior therapy should have included an anthracycline unless clinically contraindicated. |
Abraxis |
2007-02-15 |
203 |
paclitaxel |
Paxene |
treatment of advanced AIDS-related Kaposi's sarcoma after failure of first line or subsequent systemic chemotherapy |
Baker Norton Pharmaceuticals, Inc |
1997-12-24 |
204 |
paclitaxel |
Taxol |
Treatment of patients with metastatic carcinoma of the ovary after failure of first-line or subsequent chemotherapy. |
Bristol-Myers Squibb |
1992-12-29 |
205 |
paclitaxel |
Taxol |
Treatment of breast cancer after failure of combination chemotherapy for metastatic disease or relapse within 6 months of adjuvant chemotherapy. Prior therapy should have included an anthracycline unless clinically contraindicated. |
Bristol-Myers Squibb |
1994-04-13 |
206 |
paclitaxel |
Taxol |
New dosing regimen for patients who have failed initial or subsequent chemotherapy for metastatic carcinoma of the ovary |
Bristol-Myers Squibb |
1994-06-22 |
207 |
paclitaxel |
Taxol |
second line therapy for AIDS related Kaposi's sarcoma. |
Bristol-Myers Squibb |
1997-08-04 |
208 |
paclitaxel |
Taxol |
For first-line therapy for the treatment of advanced carcinoma of the ovary in combination with cisplatin. |
Bristol-Myers Squibb |
1998-04-09 |
209 |
paclitaxel |
Taxol |
for use in combination with cisplatin, for the first-line treatment of non-small cell lung cancer in patients who are not candidates for potentially curative surgery and/or radiation therapy. |
Bristol-Myers Squibb |
1998-06-30 |
210 |
paclitaxel |
Taxol |
For the adjuvant treatment of node-positive breast cancer administered sequentially to standard doxorubicin-containing combination therapy. |
Bristol-Myers Squibb |
1999-10-25 |
211 |
paclitaxel |
Taxol |
First line ovarian cancer with 3 hour infusion. |
Bristol-Myers Squibb |
2000-06-20 |
212 |
paclitaxel protein-bound particles |
Abraxane |
For the treatment of breast cancer after failure of combination chemotherapy for metastatic disease or relapse within 6 months of adjuvant chemotherapy. Prior therapy should have included an anthracyline unless clinically contraindicated |
AM Bioscience |
2005-01-07 |
213 |
palifermin |
Kepivance |
Decrease the incidence and duration of severe oral mucositis in patients with hematologic malignancies receiving myelotoxic therapy requiring hematopoetic stem cell support |
Amgen |
2004-12-15 |
214 |
pamidronate |
Aredia |
Treatment of osteolytic bone metastases of breast cancer in conjunction with standard antineoplastic therapy. |
Novartis |
1998-09-22 |
215 |
panitumumab |
Vectibix |
to treat metastatic colorectal carcinoma |
Amgen |
2006-09-27 |
216 |
pegademase |
Adagen (Pegademase Bovine) |
Enzyme replacement therapy for patients with severe combined immunodeficiency asa result of adenosine deaminase deficiency. |
Enzon |
1990-03-21 |
217 |
pegaspargase |
Oncaspar |
Acute lymphoblastic leukemia |
Enzon |
2006-07-24 |
218 |
pegaspargase |
Oncaspar |
Acute lymphocytic leukemia in L-asparaginase hypersensitive patients |
Enzon, Inc |
1994-02-01 |
219 |
Pegfilgrastim |
Neulasta |
Neulasta is indicated to decrease the incidence of infection, as manifested by febrile neutropenia, in patients with non-myeloid malignancies receiving myelosuppressive anti-cancer drugs associated with a clinically significant incidence of febrile neutropenia. |
Amgen, Inc |
2002-01-31 |
220 |
Peginterferon alfa-2b |
PegIntron |
trade name from PEG-Intron to PegIntron |
Schering |
2006-12-22 |
221 |
pemetrexed disodium |
Alimta |
For use in the treatment of patients with malignant pleural mesothelioma whose disease is either unresectable or who are otherwise not candidates for curative surgery |
Lilly |
2004-02-04 |
222 |
pemetrexed disodium |
Alimta |
Accel. Approv. (clinical benefit not established) as a single agent for the treatment of patients with locally advanced or metastatic non-small lung cancer after prior chemotherapy |
Lilly |
2004-08-19 |
223 |
pentostatin |
Nipent |
Single agent treatment for adult patients with alpha interferon refractory hairy cell leukemia. |
Parke-Davis Pharmaceutical Co. |
1991-10-11 |
224 |
pentostatin |
Nipent |
Single-agent treatment for untreated hairy cell leukemia patients with active disease as defined by clinically significant anemia, neutropenia, thrombocytopenia, or disease-related symptoms. (Supplement for front -line therapy.) |
Parke-Davis Pharmaceutical Co. |
1993-09-29 |
225 |
pipobroman |
Vercyte |
|
Abbott Labs |
1996-07-01 |
226 |
plicamycin, mithramycin |
Mithracin |
|
Pfizer Labs |
1970-05-05 |
227 |
porfimer sodium |
Photofrin |
For the ablation of high-grade dysplasia in Barrett’s esophagus patients who do not undergo esophagectomy |
Axcan Scandipharm |
2003-08-01 |
228 |
porfimer sodium |
Photofrin |
For use in photodynamic therapy (PDT) for palliation of patients with completely obstructing esophageal cancer, or patients with partially obstructing esophageal cancer who cannot be satisfactorily treated with ND-YAG laser therapy. |
QLT Phototherapeutics Inc. |
1995-12-27 |
229 |
porfimer sodium |
Photofrin |
For use in photodynamic therapy for treatment of microinvasive endobronchial nonsmall cell lung cancer in patients for whom surgery and radiotherapy are not indicated. |
QLT Phototherapeutics Inc. |
1998-01-09 |
230 |
porfimer sodium |
Photofrin |
For use in photodynamic therapy (PDT) for reduction of obstruction and palliation of symptoms in patients with completely or partially obstructing endobroncial nonsmall cell lung cancer (NSCLC). |
QLT Phototherapeutics Inc. |
1998-12-22 |
231 |
procarbazine |
Matulane |
|
Sigma Tau Pharms |
1969-07-22 |
232 |
quinacrine |
Atabrine |
|
Abbott Labs |
1964-12-07 |
233 |
Rasburicase |
Elitek |
ELITEK is indicated for the initial management of plasma uric acid levels in pediatric patients with leukemia, lymphoma, and solid tumor malignancies who are receiving anti-cancer therapy expected to result in tumor lysis and subsequent elevation of plasma uric acid. |
Sanofi-Synthelabo, Inc |
2002-07-12 |
234 |
rituximab |
Rituxan |
for the first-line treatment of patients with low grade or follicular, CD20-positive B-cell non-Hodgkin’s lymphoma. |
Genentech |
2006-09-29 |
235 |
rituximab |
Rituxan |
for the first-line treatment of patients with low grade or follicular, CD20-positive B-cell non-Hodgkin’s lymphoma. |
Genentech |
2006-09-29 |
236 |
Rituximab |
Rituxan |
Treatment of patients with relapsed or refractory low-grade or follicular B-cell non-Hodgkin's lymphoma |
Genentech, Inc |
1997-10-26 |
237 |
Rituximab |
Rituxan |
non-Hodgkin's lymphoma |
Genentech, Inc |
2006-02-10 |
238 |
sargramostim |
Leukine |
Acceleration of myeloid recovery following autologous bone marrow transplant in patients with non-Hodgkin's lymphoma, acute lymphocytic leukemia, or Hodgkin's disease |
Berlex |
1991-03-05 |
239 |
Sargramostim |
Prokine |
|
Immunex Corp |
1996-10-07 |
240 |
sorafenib |
Nexavar |
For the treatment of patients with advanced renal cell carcinoma |
Bayer |
2005-12-20 |
241 |
streptozocin |
Zanosar |
Antineoplastic agent. |
Pharmacia & Upjohn Company |
1983-05-07 |
242 |
sunitinib |
Sutent |
for the treatment of gastrointestinal stromal tumor after disease progression on or intolerance to imatinib mesylate; for the treatment of advanced renal cell carcinoma. |
CP Pharmaceuticals |
2007-02-02 |
243 |
sunitinib maleate |
Sutent |
treatment of gastrointestinal stromal tumor after disease progression on or intolerance to imatinib mesylate |
Pfizer |
2006-01-26 |
244 |
sunitinib maleate |
Sutent |
Accel. Approv. (clinical benefit not established) for the treatment of advanced renal cell carcinoma. Approval for advanced renal cell carcinoma is based on partial response rates and duration of responses. There are no randomized trials of SUTENT demonstrating clinical benefit such as increased survival or improvement in disease-related symptoms in renal cell carcinoma. |
Pfizer |
2006-01-26 |
245 |
talc |
Sclerosol |
For the prevention of the recurrence of malignant pleural effusion in symptomatic patients. |
Bryan |
1997-12-24 |
246 |
tamoxifen |
Nolvadex |
|
AstraZeneca Pharmaceuticals |
1977-12-30 |
247 |
tamoxifen |
Nolvadex |
As a single agent to delay breast cancer recurrence following total mastectomy and axillary dissection in postmenopausal women with breast cancer (T1-3, N1, M0) |
AstraZeneca Pharmaceuticals |
1986-12-03 |
248 |
tamoxifen |
Nolvadex |
For use in premenopausal women with metastatic breast cancer as an alternative to oophorectomy or ovarian irradiation |
AstraZeneca Pharmaceuticals |
1989-03-16 |
249 |
tamoxifen |
Nolvadex |
For use in women with axillary node-negative breast cancer adjuvant therapy. |
AstraZeneca Pharmaceuticals |
1990-06-21 |
250 |
tamoxifen |
Nolvadex |
Metastatic breast cancer in men. |
AstraZeneca Pharmaceuticals |
1993-04-01 |
251 |
tamoxifen |
Nolvadex |
Equal bioavailability of a 20 mg Nolvadex tablet taken once a day to a 10 mg Nolvadex tablet taken twice a day. |
AstraZeneca Pharmaceuticals |
1994-03-21 |
252 |
tamoxifen |
Nolvadex |
to reduce the incidence of breast cancer in women at high risk for breast cancer |
AstraZeneca Pharmaceuticals |
1998-10-29 |
253 |
tamoxifen |
Nolvadex |
In women with DCIS, following breast surgery and radiation, Nolvadex is indicated to reduce the risk of invasive breast cancer. |
AstraZeneca Pharmaceuticals |
2000-06-29 |
254 |
temozolomide |
Temodar |
Accel. Approv. (clinical benefit not established) Treatment of adult patients with refractory anaplastic astrocytoma, i.e., patients at first relapse with disease progression on a nitrosourea and procarbazine containing regimen |
Schering |
1999-08-11 |
255 |
temozolomide |
Temodar |
Conversion to regular approval for the treatment of patients with newly diagnosed high grade gliomas concomitantly with radiotherapy and then as adjuvant treatment |
Schering |
2005-03-15 |
256 |
teniposide, VM-26 |
Vumon |
In combination with other approved anticancer agents for induction therapy in patients with refractory childhood acute lymphoblastic leukemia (all). |
Bristol-Myers Squibb |
1992-07-14 |
257 |
testolactone |
Teslac |
|
Bristol-Myers Squibb |
1969-06-03 |
258 |
testolactone |
Teslac |
|
Bristol-Myers Squibb |
1970-05-27 |
259 |
thalidomide |
Thalomid |
Multiple myeloma |
Celgene |
2006-05-26 |
260 |
thioguanine, 6-TG |
Thioguanine |
|
GlaxoSmithKline |
1966-01-18 |
261 |
thiotepa |
Thioplex |
|
Immunex Corporation |
1959-03-09 |
262 |
thiotepa |
Thioplex |
|
Immunex Corporation |
1994-12-22 |
263 |
thiotepa |
Thioplex |
|
Lederle Laboratories |
1990-08-15 |
264 |
topotecan |
Hycamtin |
Treatment of patients with metastatic carcinoma of the ovary after failure of initial or subsequent chemotherapy. |
GlaxoSmithKline |
1996-05-28 |
265 |
topotecan |
Hycamtin |
Treatment of small cell lung cancer sensitive disease after failure of first-line chemotherapy. In clinical studies submitted to support approval, sensitive disease was defined as disease responding to chemotherapy but subsequently progressing at least 60 days (in the phase 3 study) or at least 90 days (in the phase 2 studies) after chemotherapy |
GlaxoSmithKline |
1998-11-30 |
266 |
topotecan hcl |
Hycamtin |
Cervical carcinoma |
GlaxoSmithKline |
2006-06-14 |
267 |
toremifene |
Fareston |
Treatment of advanced breast cancer in postmenopausal women. |
Orion Corp. |
1997-05-29 |
268 |
Tositumomab |
Bexxar |
Accel. Approv. (clinical benefit not established) Treatment of patients with CD20 positive, follicular, non-Hodgkin's lymphoma, with and without transformation, whose disease is refractory to Rituximab and has relapsed following chemotherapy |
Corixa Corporation |
2003-06-27 |
269 |
Tositumomab/I-131 tositumomab |
Bexxar |
Expand the indication to include patients with relapsed or refractory low grade follicular transformed CD20-positive non-Hodgkin's lymphoma who have not received rituximab |
GlaxoSmithKline |
2004-12-22 |
270 |
trastuzumab |
Herceptin |
Early Stage Breast Cancer After Primary Therapy |
Genentech |
2006-11-16 |
271 |
Trastuzumab |
Herceptin |
HERCEPTIN as a single agent is indicated for the treatment of patients with metastatic breast cancer whose tumors overexpress the HER2 protein and who have received one or more chemotherapy regimens for their metastatic disease. |
Genentech, Inc |
1998-09-25 |
272 |
Trastuzumab |
Herceptin |
Herceptin in combination with paclitaxel is indicated for treatment of patients with metastatic breast cancer whose tumors overexpress the HER-2 protein and had not received chemotherapy for their metastatic disease |
Genentech, Inc |
2000-02-09 |
273 |
Trastuzumab |
Herceptin |
|
Genentech, Inc |
2002-08-28 |
274 |
Trastuzumab |
Herceptin |
|
Genentech, Inc |
2002-08-28 |
275 |
tretinoin, ATRA |
Vesanoid |
Induction of remission in patients with acute promyelocytic leukemia (APL) who are refractory to or unable to tolerate anthracycline based cytotoxic chemotherapeutic regimens. |
Roche |
1995-11-22 |
276 |
Uracil Mustard |
Uracil Mustard Capsules |
|
Roberts Labs |
1962-09-13 |
277 |
valrubicin |
Valstar |
For intravesical therapy of BCG-refractory carcinoma in situ (CIS) of the urinary bladder in patients for whom immediate cystectomy would be associated with unacceptable morbidity or mortality. |
Anthra --> Medeva |
1998-09-25 |
278 |
vinblastine |
Velban |
|
Eli Lilly |
1965-11-05 |
279 |
vincristine |
Oncovin |
|
Eli Lilly |
1963-07-10 |
280 |
vincristine |
Oncovin |
|
Eli Lilly |
1963-07-10 |
281 |
vincristine |
Oncovin |
|
Eli Lilly |
1963-07-10 |
282 |
vincristine |
Oncovin |
|
Eli Lilly |
1963-07-10 |
283 |
vincristine |
Oncovin |
|
Eli Lilly |
1963-07-10 |
284 |
vincristine |
Oncovin |
|
Eli Lilly |
1963-07-10 |
285 |
vincristine |
Oncovin |
|
Eli Lilly |
1963-07-10 |
286 |
vinorelbine |
Navelbine |
Single agent or in combination with cisplatin for the first-line treatment of ambulatory patients with unresectable, advanced non-small cell lung cancer (NSCLC). |
GlaxoSmithKline |
1994-10-23 |
287 |
vinorelbine |
Navelbine |
Navelbine is indicated as a single agent or in combination with cisplatin for the first-line treatment of ambulatory patients with unreseactable, advanced non-small cell lung cancer (NSCLC). In patients with Stage IV NSCLC, Navelbine is indicated as a single agent or in combination with cisplatin. In Stage III NSCLC, Navelbine is indicated in combination with cisplatin. |
GlaxoSmithKline |
2002-11-05 |
288 |
vorinostat |
Zolinza |
for the treatment of cutaneous manifestations of cutaneous T-cell lymphoma (CTCL) in patients with progressive, persistent, or recurrent disease on or following two systemic therapies. |
Merck |
2006-10-06 |
289 |
zoledronate |
Zometa |
the treatment of patients with multiple myeloma and patients with documented bone metastases from solid tumors, in conjunction with standard antineoplastic therapy. Prostate cancer should have progressed after treatment with at least one hormonal therapy |
Novartis |
2002-02-22 |
290 |
zoledronic acid |
Zometa |
Treatment of hypercalcemia of malignancy |
Novartis |
2001-08-20 |