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A review of iniparib in ovarian cancer
- Source :
- Expert Opinion on Investigational Drugs. 22:399-405
- Publication Year :
- 2013
- Publisher :
- Informa Healthcare, 2013.
-
Abstract
- Patients with metastatic ovarian cancer continue to experience high recurrence rates and significant morbidity from standard treatments. There is a great need for efficacious tumor-specific agents in ovarian cancer. Iniparib (BSI-201) is a targeted drug currently under investigation.The authors identified the mechanistic and clinical data available on the role of iniparib in ovarian cancer. Iniparib was initially thought to act via the poly-ADP ribose polymerase 1 (PARP-1) pathway, but recent studies have shown only nonspecific interactions between the drug and PARP proteins. Although iniparib is only active in cancer cells, the exact mechanism of action remains unclear. Iniparib was well tolerated at all dose levels in Phase I studies of solid organ malignancies. Preliminary data from Phase II studies of iniparib for the treatment of platinum-sensitive and platinum-resistant recurrent ovarian cancer show improvement in survival compared to historic controls. There are currently no Phase III studies.Iniparib shows promise in early clinical trials; however, understanding the pathways of cytotoxicity will be crucial as cancer therapy becomes increasingly individualized.
- Subjects :
- Drug
Oncology
medicine.medical_specialty
media_common.quotation_subject
Poly (ADP-Ribose) Polymerase Inhibitor
chemistry.chemical_compound
Internal medicine
medicine
Humans
Pharmacology (medical)
media_common
Ovarian Neoplasms
Pharmacology
Clinical Trials as Topic
business.industry
General Medicine
medicine.disease
chemistry
Recurrent Ovarian Cancer
Benzamides
Cancer cell
Immunology
Female
Poly(ADP-ribose) Polymerases
Iniparib
Ovarian cancer
business
Metastatic ovarian cancer
Subjects
Details
- ISSN :
- 17447658 and 13543784
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Expert Opinion on Investigational Drugs
- Accession number :
- edsair.doi.dedup.....bf3b47eeb5e638fb41761eae198f6274
- Full Text :
- https://doi.org/10.1517/13543784.2013.772135