Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The combination of doxorubicin and veliparib represents a therapeutic approach that combines a traditional chemotherapeutic agent (doxorubicin) with a PARP inhibitor (veliparib). This combination has been studied primarily in clinical trials for various cancers, particularly breast and ovarian cancers. Veliparib (ABT-888) is a potent, oral inhibitor of PARP-1 and PARP-2 enzymes, which play crucial roles in DNA damage recognition and repair. By inhibiting these enzymes, veliparib enhances the effects of DNA-damaging agents like doxorubicin. This combination leverages the DNA-damaging effects of doxorubicin with the PARP inhibition of veliparib, which blocks DNA repair mechanisms, potentially enhancing antitumor activity particularly in BRCA-deficient cancers.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on doxorubicin + veliparib.