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Rucaparib

Generic Name
Rucaparib
Brand Names
Rubraca
Drug Type
Small Molecule
Chemical Formula
C19H18FN3O
CAS Number
283173-50-2
Unique Ingredient Identifier
8237F3U7EH

Overview

Rucaparib is an anticancer drug and poly (ADP-ribose) polymerase (PARP) inhibitor. PARP is an enzyme that plays an essential role in DNA repair. Rucaparib is proposed to work in several PARP-dependent and PARP-independent mechanisms of action; however, it causes a unique effect of synthetic lethality. By targeting the genetically-mutated cancer cells that lack a DNA repair mechanism, rucaparib causes cancer cell death and reduces tumour growth. Rucaparib was granted FDA Breakthrough Therapy designation in April 2015 and accelerated approval in December 2016. The drug was later approved by the European Commission in May 2018. It is currently used to treat recurrent ovarian and prostate cancer in adults.

Background

Rucaparib is an anticancer drug and poly (ADP-ribose) polymerase (PARP) inhibitor. PARP is an enzyme that plays an essential role in DNA repair. Rucaparib is proposed to work in several PARP-dependent and PARP-independent mechanisms of action; however, it causes a unique effect of synthetic lethality. By targeting the genetically-mutated cancer cells that lack a DNA repair mechanism, rucaparib causes cancer cell death and reduces tumour growth. Rucaparib was granted FDA Breakthrough Therapy designation in April 2015 and accelerated approval in December 2016. The drug was later approved by the European Commission in May 2018. It is currently used to treat recurrent ovarian and prostate cancer in adults.

Indication

Rucaparib is indicated for the maintenance treatment of adult patients with a deleterious BRCA mutation (germline and/or somatic)- associated recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in a complete or partial response to platinum-based chemotherapy. Under accelerated approval by the FDA, rucaparib is also indicated for the treatment of adult patients with a deleterious BRCA mutation (germline and/or somatic)-associated metastatic castration-resistant prostate cancer (mCRPC) who have been treated with androgen receptor-directed therapy and a taxane-based chemotherapy.

Associated Conditions

  • Metastatic Castration-Resistant Prostate Cancer (mCRPC)
  • Recurrent Epithelial Ovarian Cancer
  • Recurrent Fallopian Tube Cancer
  • Recurrent Primary Peritoneal Cancer

FDA Approved Products

Rubraca
Manufacturer:pharmaand GmbH
Route:ORAL
Strength:200 mg in 1 1
Approved: 2023/09/30
NDC:82154-0783
Rubraca
Manufacturer:pharmaand GmbH
Route:ORAL
Strength:250 mg in 1 1
Approved: 2023/09/30
NDC:82154-0784
Rubraca
Manufacturer:pharmaand GmbH
Route:ORAL
Strength:300 mg in 1 1
Approved: 2023/09/30
NDC:82154-0785

Singapore Approved Products

No Singapore products found for this drug

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