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Carboplatin

Generic Name
Carboplatin
Brand Names
Paraplatin
Drug Type
Small Molecule
Chemical Formula
C6H12N2O4Pt
CAS Number
41575-94-4
Unique Ingredient Identifier
BG3F62OND5

Overview

Carboplatin is an organoplatinum antineoplastic alkylating agent used in the treatment of advanced ovarian carcinoma. Early clinical studies of carboplatin were performed in 1982. Carboplatin was developed as an analog of cisplatin with reduced nephrotoxicity and vomiting. Carboplatin was granted FDA approval on 3 March 1989.

Background

Carboplatin is an organoplatinum antineoplastic alkylating agent used in the treatment of advanced ovarian carcinoma. Early clinical studies of carboplatin were performed in 1982. Carboplatin was developed as an analog of cisplatin with reduced nephrotoxicity and vomiting. Carboplatin was granted FDA approval on 3 March 1989.

Indication

Carboplatin is indicated in combination with an established combination of chemotherapeutic agents for the initial treatment of advanced ovarian carcinoma. Carboplatin is also indicated for the palliative treatment of ovarian carcinoma, recurrent after prior chemotherapy.

Associated Conditions

  • Advanced Cervical Cancer
  • Advanced Endometrial Cancer
  • Advanced Esophageal Cancers
  • Advanced Head and Neck Cancer
  • Advanced Melanoma
  • Advanced Non-Small Cell Lung Cancer (NSCLC)
  • Advanced Ovarian Carcinoma
  • Advanced Sarcoma
  • Malignant Pleural Mesothelioma (MPM)
  • Merkel Cell Carcinoma
  • Metastatic Breast Cancer
  • Refractory Hodgkin Lymphoma
  • Retinoblastoma
  • Thymoma
  • Advanced Bladder cancer
  • Advanced Small cell lung cancer
  • Advanced Testicular cancer
  • Advanced Thymoma
  • Refractory Non-Hodgkin's lymphoma

Clinical Trials

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Title
Posted
Study ID
Phase
Status
Sponsor
2003/04/03
Phase 2
Completed
2003/03/07
Phase 2
Completed
2003/03/07
Phase 3
UNKNOWN
2003/03/07
Phase 2
Completed
2003/03/07
Phase 3
Withdrawn
2003/02/06
Phase 3
Terminated
2003/02/06
Phase 3
Withdrawn
2003/01/28
Phase 2
Completed
2003/01/28
Phase 1
Completed
2003/01/27
Phase 1
Completed

FDA Approved Products

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NMPA Approved Products

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