Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The IPGDP regimen is a five-drug combination chemotherapy protocol consisting of ifosfamide, pegaspargase, gemcitabine, cisplatin, and dexamethasone. It is being developed and evaluated by the Chinese Academy of Medical Sciences for the treatment of extranodal natural killer/T-cell lymphoma (ENKL), nasal type. This aggressive malignancy is strongly associated with Epstein-Barr virus and often exhibits multidrug resistance. The IPGDP regimen aims to overcome this resistance by combining agents with distinct mechanisms: gemcitabine (a pyrimidine antimetabolite), ifosfamide (an alkylating agent), cisplatin (a platinum-based DNA crosslinker), pegaspargase (an enzyme that depletes L-asparagine), and dexamethasone (a corticosteroid). The regimen is currently in Phase II clinical trials (NCT02560441), where it is being tested in combination with radiotherapy for early-stage disease and as a standalone therapy for advanced or relapsed/refractory ENKL.
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 ifosfamide + pegaspargase + gemcitabine + cisplatin + dexamethasone.