- |||||||||| NC410 / NextCure
Enrollment change, Trial completion date, Trial termination, Trial primary completion date, Metastases: A Safety and Tolerability Study of NC410 in Subjects With Advanced or Metastatic Solid Tumors (clinicaltrials.gov) - Aug 14, 2023 P1/2, N=46, Terminated, Thus, additional targeting of the LAIR-1:collagen pathway with NC410 is a promising approach to treating tumours where conventional immunotherapy is ineffective. N=128 --> 46 | Trial completion date: Dec 2023 --> Jul 2023 | Active, not recruiting --> Terminated | Trial primary completion date: Dec 2023 --> Jul 2023; Upon completion of the Phase 1 portion of the NC410 monotherapy trial, NextCure focused efforts on a combination trial of NC410 in solid tumors.
- |||||||||| NC410 / NextCure
Enrollment closed, Metastases: A Safety and Tolerability Study of NC410 in Subjects With Advanced or Metastatic Solid Tumors (clinicaltrials.gov) - Apr 10, 2023 P1/2, N=128, Active, not recruiting, N=128 --> 46 | Trial completion date: Dec 2023 --> Jul 2023 | Active, not recruiting --> Terminated | Trial primary completion date: Dec 2023 --> Jul 2023; Upon completion of the Phase 1 portion of the NC410 monotherapy trial, NextCure focused efforts on a combination trial of NC410 in solid tumors. Recruiting --> Active, not recruiting
- |||||||||| NC410 / NextCure, Keytruda (pembrolizumab) / Merck (MSD)
A phase 1b/2, open-label, safety, tolerability and efficacy study of NC410 plus pembrolizumab for participants with immune checkpoint inhibitor (ICI) refractory, or MSS/MSI-low ICI naïve advanced or metastatic solid tumors (Hall C) - Oct 6, 2022 - Abstract #SITC2022SITC_1056; Objective response rate (ORR) based on RECIST v1.1 will be the primary endpoint, while duration of response (DoR), disease control rate (DCR), progression-free survival (PFS), and overall survival will be evaluated as secondary endpoints. Several biomarker effects of NC410 in combination with pembrolizumab in peripheral blood and tumor tissue will be assessed.
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