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NCT07293754From ClinicalTrials.govRecruiting

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

A Phase 1/2 Trial of RPTR-1-201, a T Cell Receptor Bispecific Therapy, in Advanced Solid Tumors

  • Advanced Malignant Solid Tumor

At a glance

Phase
Phase 1
Study type
Interventional
Sponsor
Repertoire Immune Medicines
Enrolment target
150
Started
12 December 2025
Main results due
15 December 2028
Study sites
12
Registry updated
28 September 2026

Can you take part?

  • Aged 18 years and over.
  • Open to any sex.
  • You need the condition being studied — healthy volunteers are not accepted.

These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.

Read the full eligibility criteria
Inclusion Criteria

* Histologically or cytologically confirmed locally advanced or metastatic solid tumors that is not amenable to curative treatment.
* At least one measurable lesion per 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.

Exclusion Criteria:

* History of another malignancy within 3 years before the first dose of trial intervention, with the exception of malignancies considered cured and not expected to require active therapy (for example, certain skin cancers or in situ malignancies) per protocol.
* 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 condition, that in the opinion of the investigator, would increase risk or interfere with trial participation.
* Other protocol-defined inclusion and exclusion criteria apply

What this study is about

In the sponsor’s own words, from the registry.

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.

Study sites(12)

  • START Midwest

    Grand Rapids, Michigan, United States

    Recruiting

  • START New York-Long Island

    Lake Success, New York, United States

    Recruiting

  • START San Antonio

    San Antonio, Texas, United States

    Recruiting

  • START Dublin

    Dublin, Ireland

    Recruiting

  • START Lisbon

    Lisbon, Portugal

    Recruiting

  • START Barcelona

    Barcelona, Spain

    Recruiting

  • START Rioja

    Logroño, Spain

    Recruiting

  • Clinica Universidad de Navarra - Madrid

    Madrid, Spain

    Recruiting

  • START Madrid-CIOCC

    Madrid, Spain

    Recruiting

  • START Madrid-FJD

    Madrid, Spain

    Recruiting

  • Clinica Universidad de Navarra - Pamplona

    Pamplona, Spain

    Recruiting

  • INCLIVA Instituto de Investigación Sanitaria VLC

    Valencia, Spain

    Recruiting

Showing 12 of 12 sites. 12 of the 12 sites on this study are recruiting right now — a site can stop enrolling while the study as a whole is still open.

Source: ClinicalTrials.gov record NCT07293754. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.

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