Drug intelligence / Profile preview

olaparib + rifampicin

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Small Molecules
Administration
Oral
01

Overview

**Olaparib + rifampicin** is not a fixed-dose combination product but refers to the concurrent administration of the two drugs. **Olaparib** is a small molecule PARP (poly(ADP-ribose) polymerase) inhibitor used primarily in the treatment of various cancers, notably ovarian and breast cancer, by interfering with DNA repair in cells with homologous recombination repair deficiency. **Rifampicin** is a potent antibiotic and a strong inducer of CYP3A4. When administered together, rifampicin significantly induces the metabolism of olaparib, leading to a marked reduction (around 87%) in olaparib’s systemic exposure, which can compromise its efficacy. The combination is generally contraindicated due to this strong pharmacokinetic interaction[1][3][5]. **Olaparib developer:** AstraZeneca. **Rifampicin developer:** Originally developed by the Italian company Lepetit.

Other names
olaparibrifampicinrifampin
02

Targets

UGT1A1 (UDP-glucuronosyltransferase 1A1)RNAP (Bacterial dna-dependent RNA polymerase)ABCB1 (P-glycoprotein)

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