- |||||||||| perenostobart (SRF617) / Coherus Biosci
Trial completion, Enrollment change, Metastases: KEYNOTE-A62: Study of SRF617 in Patients With Advanced Solid Tumors (clinicaltrials.gov) - Aug 28, 2023 P1, N=85, Completed, Completed --> Terminated; The study was terminated for strategic reasons, not due to any safety concerns. Active, not recruiting --> Completed | N=177 --> 85
- |||||||||| perenostobart (SRF617) / Coherus Biosci
Enrollment closed, Trial completion date, Trial primary completion date, Combination therapy, Metastases: Study of SRF617 With AB928 (Etrumadenant) and AB122 (Zimberelimab) in Patients With Metastatic Castration Resistant Prostate Cancer (clinicaltrials.gov) - Nov 30, 2022 P2, N=40, Active, not recruiting, Active, not recruiting --> Completed | N=40 --> 15 Recruiting --> Active, not recruiting | Trial completion date: Nov 2023 --> Jul 2023 | Trial primary completion date: Nov 2023 --> May 2023
- |||||||||| perenostobart (SRF617) / Coherus Biosci
Enrollment closed, Trial completion date, Trial primary completion date, Metastases: KEYNOTE-A62: Study of SRF617 in Patients With Advanced Solid Tumors (clinicaltrials.gov) - Nov 30, 2022 P1, N=177, Active, not recruiting, Recruiting --> Active, not recruiting | Trial completion date: Nov 2023 --> Jul 2023 | Trial primary completion date: Nov 2023 --> May 2023 Recruiting --> Active, not recruiting | Trial completion date: Nov 2022 --> Oct 2023 | Trial primary completion date: Oct 2022 --> Aug 2023
- |||||||||| SRF617 / Surface Oncology
First-in-human phase 1 trial of SRF617, a potent inhibitor of CD39 activity, as monotherapy or in combination, in patients (pts) with advanced solid tumors. (Foyer ABC [VIRTUAL]) - Oct 29, 2021 - Abstract #ESMOIO2021ESMO_IO_265; P1 Methods Pts with advanced solid tumors were enrolled in a phase 1 dose-escalation study of SRF617 (NCT04336098) to establish preliminary safety as monotherapy as well as in combination with gemcitabine + nab-paclitaxel (GA) or pembrolizumab (P) and to identify doses suitable for monotherapy and combination expansion cohorts...Legal entity responsible for the study Surface Oncology, Cambridge, MA, USA. Funding Surface Oncology, Cambridge, MA, USA.
- |||||||||| SRF617 / Surface Oncology
The fully human antibody SRF617 is a potent inhibitor of ecto-enzyme CD39 in vivo (Poster Hall) - Oct 1, 2021 - Abstract #SITC2021SITC_330; P1 These studies demonstrate the therapeutic potential of targeting CD39 for the treatment of cancer. SRF617 is currently being evaluated in a Phase 1 clinical trial in patients with advanced solid tumors (NCT04336098) and in combination with chemotherapy in patients with pancreatic cancer.
- |||||||||| perenostobart (SRF617) / Coherus Biosci
Enrollment change, Metastases: KEYNOTE-A62: Study of SRF617 in Patients With Advanced Solid Tumors (clinicaltrials.gov) - Dec 19, 2020 P1, N=100, Recruiting, SRF617 is currently being evaluated in a Phase 1 clinical trial in patients with advanced solid tumors (NCT04336098) and in combination with chemotherapy in patients with pancreatic cancer. N=56 --> 100
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