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Study identifier: NCT07156136 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Recruiting

Study of IMC-P115C in Advanced PRAME-Positive Cancers

Condition: PRAME Positive · Cancer · HLA-A*02:01-positive  ·  Sponsor: Immunocore Ltd

PhasePhase 1
Planned participants140
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where13 locations · 4 countries

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

Phase 1 First-in-human study of the safety and efficacy of IMC-P115C as a single agent and in combination with standard of care (SOC) agents in participants with advanced PRAME positive cancers. IMC-P115C is a half-life extended (HLE) ImmTAC targeting PRAME.

This description comes directly from the study's public registry record.

Talk to the study team

Immunocore Medical Information Global  ·  844-466-8661  ·  medical.information@immunocore.com

Immunocore Medical Information EU  ·  +00 800-744-51111  ·  medinfo.eu@immunocore.com

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1 * HLA-A\*02:01-positive * Meeting PRAME-positive tumor testing requirements * Metastatic or unresectable solid tumors * Have received (or be receiving), relapsed from, be refractory to or intolerant of all therapies * Male and female participants of childbearing potential who are sexually active with a non-sterilized partner must agree to use highly effective methods of birth control Exclusion Criteria: * Symptomatic or untreated central nervous system metastasis * Bowel obstruction, perforation, or fistula formation within 3 months prior to the planned first dose of study treatment * Ongoing ascites or effusion requiring recent drainages * Significant ongoing toxicity from prior anticancer treatment * Out-of-range laboratory values * Clinically significant lung, heart, or autoimmune disease * Ongoing requirement for immunosuppressive treatment * Significant secondary malignancy * Hypersensitivity to study drug or excipients * Pregnant or lactating

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (13)

Cancer Research South Australia (CRSA)Adelaide, AustraliaRecruiting
Linear Clinical Research ltd.Nedlands, AustraliaRecruiting
Melanoma Institute AustraliaWollstonecraft, AustraliaRecruiting
UNICANCER - Centre Leon-Berard (CLB)Lyon, FranceRecruiting
Centre Hospitalier Universitaire (CHU) de Toulouse-Institut Universitaire du Cancer de Toulouse-Oncopole (IUCT-Oncopole)Toulouse, FranceRecruiting
Institut Gustave RoussyVillejuif, FranceRecruiting
Fondazione IRCCS - Istituto Nazionale dei TumoriMilan, ItalyRecruiting
Istituto Europeo di OncologiaMilan, ItalyRecruiting
Istituto Nazionale Tumori IRCCS Fondazione "G. Pascale"Naples, ItalyRecruiting
Hospital Universitari Vall d HebronBarcelona, SpainRecruiting
Institut Catala d'Oncologia (ICO) - Hospital Duran i ReynalsBarcelona, SpainRecruiting
Hospital Universitario Ramon y CajalMadrid, SpainRecruiting

+ 1 more locations — full list on the registry record.

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

AdelaideNedlandsWollstonecraftLyon

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