ASP1012
/ KaliVir, Astellas
- LARVOL DELTA
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March 26, 2025
Trial in progress: Phase 1 study of an oncolytic virus, ASP1012, in adults with advanced solid tumors
(AACR 2025)
- P1 | "ASP1012, a double-stranded DNA oncolytic and immunotherapeutic vaccinia virus encoding a leptin-interleukin 2 fusion protein that selectively replicates in cancer cells, is being developed for the treatment of patients with locally advanced or metastatic (la/m) solid tumors. This Phase 1, first-in-human, open-label, multicenter dose escalation (Part 1) and dose expansion (Parts 2/3) study (NCT06171178) of ASP1012 alone or + pembrolizumab will evaluate the safety, tolerability, maximum tolerated dose (MTD), and/or recommended Phase 2 dose (RP2D) in US adults...Safety follow-up will occur 30 days posttreatment, posttreatment follow-up every 6 weeks, and survival follow-up ≥ every 12 weeks ± 2 weeks. Study enrollment is currently ongoing in the US."
Clinical • IO biomarker • Metastases • Oncolytic virus • P1 data • Colorectal Cancer • Cutaneous Melanoma • Gastric Cancer • Melanoma • Oncology • Ovarian Cancer • Solid Tumor • IL2 • LEP
January 04, 2024
A Study of ASP1012 in Adults With Solid Tumors
(clinicaltrials.gov)
- P1 | N=229 | Recruiting | Sponsor: Astellas Pharma Global Development, Inc. | Not yet recruiting ➔ Recruiting
Enrollment open • Metastases • Oncolytic virus • Gastric Cancer • Gastrointestinal Cancer • Melanoma • Oncology • Solid Tumor
December 14, 2023
A Study of ASP1012 in Adults With Solid Tumors
(clinicaltrials.gov)
- P1 | N=229 | Not yet recruiting | Sponsor: Astellas Pharma Global Development, Inc.
New P1 trial • Gastric Cancer • Gastrointestinal Cancer • Melanoma • Oncology • Solid Tumor
October 24, 2023
KaliVir Immunotherapeutics Announces FDA Clearance of Investigational New Drug (IND) for Systemic Oncolytic Virus ASP1012 for Phase I Clinical Trials for Locally Advanced or Metastatic Solid Tumors
(Businesswire)
- "KaliVir Immunotherapeutics, Inc...announced clearance of an Investigational New Drug (IND) application by the United States Food and Drug Administration (FDA) to initiate a Phase 1 clinical study of ASP1012 in participants with locally advanced or metastatic solid tumors....The trial is expected to begin in Q1 2024."
IND • New P1 trial • Oncology • Solid Tumor
May 23, 2022
KaliVir Immunotherapeutics Enters into Global Exclusive Licensing Agreement with Roche for Novel Oncolytic Viruses
(PRNewswire)
- "KaliVir Immunotherapeutics...announced a collaboration and global exclusive licensing agreement with Roche for the discovery, development and commercialization of novel oncolytic vaccinia viruses derived from KaliVir's oncolytic immunotherapy VETTM platform....Under the terms of the agreement, KaliVir will generate oncolytic vaccinia virus product candidates derived from the company's VETTM platform expressing Roche proprietary therapeutic transgenes. Roche will have exclusive license to discover, develop and commercialize the products worldwide. KaliVir will receive an upfront payment, and may be eligible to receive research, development and commercial milestone payments..."
Licensing / partnership • Oncology
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