Actively Recruiting

Phase 1
Phase 2
Age: 18Years +
All Genders
NCT07293754

An Early Phase Trial of RPTR-1-201 in Advanced Solid Tumors

Led by Repertoire Immune Medicines · Updated on 2026-02-17

150

Participants Needed

1

Research Sites

174 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is an early phase trial designed to evaluate the safety, tolerability, and preliminary antitumor activity of RPTR-1-201 in adults with advanced solid tumors. The trial includes dose escalation and dose expansion parts and will evaluate RPTR-1-201 as monotherapy and in combination with an anti-PD-1 monoclonal antibody.

CONDITIONS

Official Title

An Early Phase Trial of RPTR-1-201 in Advanced Solid Tumors

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Histologically or cytologically confirmed locally advanced or metastatic solid tumors that are not treatable with curative intent.
  • At least one measurable lesion according to RECIST v1.1 as assessed by the investigator.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  • Adequate organ function as defined in the trial protocol.
  • Ability to provide written informed consent and comply with trial procedures.
Not Eligible

You will not qualify if you...

  • History of another malignancy within 3 years prior to the first dose of trial treatment, except certain cured skin cancers or in situ malignancies.
  • Known active leptomeningeal disease or uncontrolled central nervous system metastases.
  • Active, clinically significant autoimmune diseases requiring systemic immunosuppressive therapy.
  • Prior allogenic organ transplantation.
  • Clinically significant uncontrolled medical or psychiatric conditions that may increase risk or interfere with trial participation.
  • Other protocol-defined inclusion and exclusion criteria apply.

AI-Screening

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Trial Site Locations

Total: 1 location

1

START Midwest

Grand Rapids, Michigan, United States, 49546

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

NON_RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

2

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