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DRUG:

liposomal gemcitabine (FF-10832)

i
Other names: FF-10832, F832
Associations
Company:
Fujifilm Holdings
Drug class:
DNA polymerase inhibitor
Associations
2ms
A Phase 1 Dose-escalation Study of FF-10832 for Treatment of Solid Tumors Including Biliary Tract Cancer (clinicaltrials.gov)
P1, N=90, Active, not recruiting, Fujifilm Pharmaceuticals U.S.A., Inc. | Recruiting --> Active, not recruiting | Trial completion date: Jun 2025 --> Dec 2025 | Trial primary completion date: Dec 2024 --> Jun 2025
Enrollment closed • Trial completion date • Trial primary completion date • Metastases
|
liposomal gemcitabine (FF-10832)
5ms
A Phase 1 Dose-escalation Study of FF-10832 for Treatment of Solid Tumors Including Biliary Tract Cancer (clinicaltrials.gov)
P1, N=90, Recruiting, Fujifilm Pharmaceuticals U.S.A., Inc. | Trial completion date: Mar 2025 --> Jun 2025 | Trial primary completion date: Sep 2024 --> Dec 2024
Trial completion date • Trial primary completion date • Metastases
|
liposomal gemcitabine (FF-10832)
11ms
Enrollment change • Combination therapy • Metastases
|
Keytruda (pembrolizumab) • liposomal gemcitabine (FF-10832)
1year
KEYNOTE-B57: A Study to Evaluate Safety, Efficacy of FF-10832 in Combination With Pembrolizumab in Solid Tumors (clinicaltrials.gov)
P2, N=10, Recruiting, Fujifilm Pharmaceuticals U.S.A., Inc. | Phase classification: P2a --> P2
Phase classification • Combination therapy • Metastases
|
Keytruda (pembrolizumab) • liposomal gemcitabine (FF-10832)