About the SKYBRIDGE Trial
Trial Name: An Open-label, Multicenter, Dose Escalation, and Dose Expansion Phase 1/2 Study with Peluntamig (PT217) Followed by a Key ChemotherapY And/or Checkpoint Inhibitor ComBination in Patients with NeuRoendocrIne Carcinomas That Are Known to Be DLL3 ExpressinG CancErs (SKYBRIDGE)
ClinicalTrials.gov Identifier: NCT05652686
Sponsor: Phanes Therapeutics
Recruitment Contact: Phanes Therapeutics, clinical-trials@phanestx.com, 858-766-0852
Completion Date: August 2028
A clinical trial evaluating peluntamig (PT217) with chemotherapy for the treatment of small cell lung cancer (SCLC) and neuroendocrine carcinoma (NEC) has dosed its first patient.1
Peluntamig is a first-in-class native IgG-like bispecific antibody that targets DLL3 and CD47. The agent is currently being developed as a potential treatment for patients with SCLC and NEC, including neuroendocrine prostate cancer (NEPC).
The FDA has already granted peluntamig 2 orphan drug designations for the treatment of SCLC and NEC, as well as 2 fast track designations for the treatment of extensive-stage small cell lung cancer (ES-SCLC) with disease progression following treatment with platinum chemotherapy with or without a checkpoint inhibitor, and metastatic de novo or treatment-emergent neuroendocrine prostate cancer (NEPC), respectively.
Last year, Phanes Therapeutics, Inc., the drug developer, entered into a clinical supply agreement with Roche to study the combination of peluntamig and the anti–PD-L1 therapy atezolizumab (Tecentriq).
The phase 1/2, multicenter SKYBRIDGE trial (NCT05652686) is currently investigating peluntamig’s safety, tolerability, pharmacokinetics, and preliminary efficacy in patients with advanced or refractory cancers expressing DLL3.2 The study is recruiting patients across sites in Colorado, Massachusetts, North Carolina, Oklahoma, Texas, and Virginia.
Enrollment is open to patients with measurable disease by RECIST v1.1, an ECOG performance status of 0 or 1, adequate organ function, resolution of adverse events from prior therapies, and a life expectancy of at least 3 months. Patients who are pregnant or lactating, have autoimmune disease, have a known concurrent malignancy, or have uncontrolled hypertension are not eligible for enrollment in the study.