Phanes Therapeutics announces first patient dosed in clinical study of peluntamig in combination with atezolizumab

SAN DIEGO, May 5, 2025 /PRNewswire/ — Phanes Therapeutics, Inc. (Phanes), a clinical stage biotech company focused on innovative drug discovery and development in oncology, announced today that the first patient has been dosed in the clinical study of peluntamig in combination with Roche’s anti-PD-L1 monoclonal antibody atezolizumab (TECENTRIQ® ). The study is being conducted in a cohort […]

Phanes Therapeutics announces first patient dosed in clinical study of peluntamig (PT217) in combination with chemotherapy

SAN DIEGO, Feb. 19, 2025 /PRNewswire/ — Phanes Therapeutics, Inc. (Phanes), a clinical stage biotech company focused on innovative drug discovery and development in oncology, announced today that the first patient has been dosed in the clinical study of peluntamig (PT217) in combination with chemotherapy. Peluntamig (PT217), a first-in-class native IgG-like bispecific antibody (bsAb) targeting DLL3 and […]

Phanes Therapeutics’ PT217 granted Fast Track designation by the FDA for NEPC

This is the second Fast Track Designation granted to PT217 by the agency SAN DIEGO, Dec. 4, 2024 /PRNewswire/ — Phanes Therapeutics, Inc. (Phanes), a clinical stage biotech company focused on innovative drug discovery and development in oncology, announced today that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to PT217 for the […]

Phanes Therapeutics announces the appointment of gastrointestinal oncologist Prof. Zev Wainberg to its Clinical Advisory Board

SAN DIEGO, Nov. 5, 2024 /PRNewswire/ — Phanes Therapeutics, Inc. (Phanes), a clinical stage biotech company focused on innovative drug discovery and development in oncology, announced today that Zev Wainberg, MD, an internationally renowned medical oncologist and professor at David Geffen School of Medicine at UCLA, has joined the Company’s Clinical Advisory Board (CAB). “We are excited to have […]

Phanes Therapeutics announces first patient dosed in clinical study of PT886 in combination with KEYTRUDA® (pembrolizumab)

SAN DIEGO, Oct. 8, 2024 /PRNewswire/ — Phanes Therapeutics, Inc. (Phanes), a clinical stage biotech company focused on innovative drug discovery and development in oncology, announced today that the first patient has been dosed in the clinical study of PT886 in combination with Merck’s anti-PD-1 therapy, KEYTRUDA® (pembrolizumab). The dosing was conducted in a cohort of gastric and […]

Phanes Therapeutics’ PT217 receives Orphan Drug designation for neuroendocrine carcinoma from the FDA

SAN DIEGO, Aug. 16, 2024 /PRNewswire/ — Phanes Therapeutics, Inc. (Phanes), a clinical stage biotech company focused on innovative drug discovery and development in oncology, announced today that the U.S. Food and Drug Administration (FDA) has granted orphan drug designation (ODD) to PT217 for the treatment of neuroendocrine carcinoma (NEC). PT217 is a first-in-class bispecific antibody targeting […]

Phanes Therapeutics, Inc. announces clinical supply agreement with Roche to evaluate PT217 in combination with an anti-PD-L1 therapy

PT217 is Phanes’ first-in-class bispecific antibody targeting DLL3 and CD47; atezolizumab (TECENTRIQ®) is Roche’s anti-PD-L1 monoclonal antibody The clinical supply agreement will focus on evaluating PT217 in combination with atezolizumab for the treatment of small cell lung cancer (SCLC), large cell neuroendocrine carcinoma of the lung (LCNEC) and extrapulmonary neuroendocrine carcinomas (EP-NECs) PT217 was recently granted Fast Track designation by the […]

Phanes Therapeutics’ PT217 granted Fast Track designation by the FDA

SAN DIEGO, April 8, 2024 /PRNewswire/ — Phanes Therapeutics, Inc. (Phanes), a clinical stage biotech company focused on innovative drug discovery and development in oncology, announced today that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to PT217 for the treatment of patients with extensive-stage small cell lung cancer (ES-SCLC) with disease progression following […]

Phanes Therapeutics’ PT886 granted Fast Track designation for the treatment of patients with metastatic claudin 18.2-positive pancreatic adenocarcinoma by the FDA

SAN DIEGO, March 20, 2024 /PRNewswire/ — Phanes Therapeutics, Inc. (Phanes), a clinical stage biotech company focused on innovative drug discovery and development in oncology, announced today that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to PT886 for the treatment of patients with metastatic claudin 18.2-positive pancreatic adenocarcinoma. PT886 was also granted […]