CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 49 enrolled
Drug / intervention
SL-279252drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03894618
NCT03894618Phase 1Completed

Phase 1 Dose Escalation and Dose Expansion Study of an Agonist Redirected Checkpoint Fusion Protein, SL-279252 (PD1-Fc-OX40L), in Subjects With Advanced Solid Tumors or Lymphomas

Shattuck Labs, Inc.·interventional·Posted Mar 28, 2019·Updated Apr 2, 2025

In Brief

A Phase 1 clinical trial evaluating SL-279252 for Squamous Cell Carcinoma of the Head and Neck and 12 related conditions. Completed, enrolled 49 participants across 5 sites in 4 countries.

Detailed Summary

This is a Phase 1 first in human, open label, multi-center, dose escalation and dose expansion study to evaluate the safety, tolerability, PK, anti-tumor activity and pharmacodynamic effects of SL-279252 in subjects with advanced solid tumors or lymphomas.

Study Details

Timeline

Phase 1CompletedFinished
2020202120222023202420252026
First PostedMar 28, 2019
Enrollment StartMar 26, 2019
Primary CompletionMay 4, 2023
TodayJul 2, 2026
Enrollment to primary: 4.1 yearsPosted 7.3 years ago

Interventions

SL-279252drug

The investigational product (IP), SL-279252, is a first-in-class agonist redirected checkpoint (ARC) fusion protein (FP) consisting of the extracellular domains of human programmed cell death 1 (PD- 1) and OX40L, linked by a central Fc domain (PD1-Fc-OX40L).