NCT07145450RecruitingPhase 1/2
Master Protocol of TCR-modified T Cell Therapy Targeting HLA-restricted KRAS Antigen Administered in Adult Patients With Metastatic or Locally Advanced PDAC
Phase 1/2 Master Protocol for Open-Label, Multi-Centre, Single-Arm Sub-Studies, First in Human Clinical Studies of TCR-T Therapy (Autologous TCR- Modified T-Cell Therapy) Targeting Mutated Kirsten Rat Sarcoma (mutKRAS) Administered in Metastatic or Locally Advanced Pancreatic Ductal Adenocarcinoma (PDAC) Adult Patients With Specific mutKRAS and Human Leukocyte Antigen (HLA) Genotypes
Source: ClinicalTrials.gov · Last updated 8 Jun 2026
Brief summary (registry, in English)
This is an open-label, multi-centre, single-arm Phase 1/2 clinical trial of the safety, expansion, persistence and clinical activity of a set of engineered autologous T cells products each capable of recognizing a specific combination mutated KRAS and HLA, activating the T cells and exerting anti- tumour activity in patients with metastatic or locally advanced PDAC.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 1/2
- Study type
- Interventional
- Enrollment
- 96 (estimated)
- First submitted
- 9 Jul 2025
- Start date
- 3 Jul 2025
- Primary completion date
- 2 Apr 2030
- Lead sponsor
- Anocca AB
- Diseases
- Sarcoma
- NCT number
- NCT07145450
What you commit to
- Study type: Interventional · Phase 1/2
- Planned participants: 96
- From 3 Jul 2025 to the primary completion date, 2 Apr 2030
- 10 sites in 4 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Another malignancy other than PDAC.
- Current or history of brain metastasis.
Other
- Patient with known genetic status for whom other treatments are available e.g. BRCA, MSI-H.
Who the study is looking for
- Adult patient (18 years or older) with newly diagnosed metastatic PDAC or locally advance PDAC disease.
- HLA genotyping confirmed with a high-resolution method.
- Confirmed KRAS G12V or KRAS G12D mutation in tumour using biopsy sample.
- Fertile male and female patients must use a highly effective contraceptive method before, during, and for at least 6 months after the last mutKRAS TCR infusion. Acceptable contraception for women includes implants, injectables, combined oral contraceptives, intrauterine devices (IUDs), sexual abstinence, or a partner who has been vasectomized for at least 6 months. Acceptable contraception for male includes having had a vasectomy for at least 6 months, sexual abstinence, to condoms plus spermicide. Fertile female and male patients must adhere to any treatment-specific pregnancy prevention guidelines for cyclophosphamide (refer to SmPC).
- Confirmed clinical benefit to SoC treatments and absence of disease progression according to the PI judgement.
- Measurable disease by RECIST 1.1 criteria at the time of first treatment. Baseline imaging (for example, diagnostic CT of chest/abdomen/pelvis and imaging of the affected extremity or brain, as appropriate), or magnetic resonance imaging (MRI) must be obtained within 8 weeks of the first planned T cell infusion. CT can be substituted for MRI in patients unable to have CT contrast.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (10)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Charité Universitätsmedizin Berlin Coordinator of this site? Confirm its status | Berlin | Germany | Recruiting |
| Technische Universitaet Dresden - Universitaetsklinikum Carl Gustav Carus Coordinator of this site? Confirm its status | Dresden | Germany | Recruiting |
| Universitaetsklinikum Heidelberg Coordinator of this site? Confirm its status | Heidelberg | Germany | Recruiting |
| Universitaetsklinikum Leipzig - Universitaeren Krebszentrum (UCCL) Coordinator of this site? Confirm its status | Leipzig | Germany | Not yet recruiting |
| Ludwig-Maximilians-Universitaet Muenchen (LMU) Klinikum der Universitaet Muenchen - Campus Grosshadern - Medizinische Klinik und Poliklinik III Coordinator of this site? Confirm its status | München | Germany | Not yet recruiting |
| University Hospital and Faculty of Medicine Eberhard Karls University Tübingen Coordinator of this site? Confirm its status | Tübingen | Germany | Recruiting |
| Herlev and Gentofte University Hospital Coordinator of this site? Confirm its status | Copenhagen | Denmark | Recruiting |
| Amsterdam UMC - VU Medical Center Coordinator of this site? Confirm its status | Amsterdam | Netherlands | Recruiting |
| Radboud University Medical Center Coordinator of this site? Confirm its status | Nijmegen | Netherlands | Recruiting |
| Karolinska University Hospital Coordinator of this site? Confirm its status | Stockholm | Sweden | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.