Phase 2 Pancreatic Cancer Trial, Recruiting NCT05985655 Sponsor: Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc. Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT05985655
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are reasonably well and able to carry out daily activities with little or no limitation (as measured by a standard medical scale called ECOG, scored 0 or 1).
  • People with a life expectancy of more than 3 months.
  • People who have been confirmed (through tissue or cell testing) to have one of the following advanced cancers: head and neck squamous cell carcinoma, pancreatic adenocarcinoma, non-small cell lung cancer, hormone receptor-positive and HER2-negative breast cancer that has stopped responding to a specific type of prior treatment (CDK4/CDK6 inhibitor), platinum-resistant high-grade ovarian, peritoneal, or fallopian tube cancer, or triple negative breast cancer.
  • People whose cancer is advanced, has come back, or has spread, and where surgery or radiotherapy are no longer considered potentially curative, after having received standard treatments.
  • People whose blood, liver, and kidney function are at adequate levels.
  • People who have at least one tumour that can be safely biopsied (a small tissue sample taken for testing), not including tumours in the bone.

Who may not be able to join:

  • People who currently have an active and serious infection.
  • People who have persistent nausea or vomiting, a long-term digestive condition, or who have had significant bowel surgery that could prevent the study drug from being properly absorbed.
  • People who have cancer that has spread to the brain or spinal cord and is causing symptoms.
  • People who have or have previously had another separate cancer.
  • People who have previously had an organ transplant or a stem cell transplant from a donor.
  • People with moderate or severe heart or blood vessel disease.
  • People who have received any cancer treatment within 28 days (or within a shorter window based on how long the drug stays in the body) before the first dose of the study drug.
  • People who have taken certain medications that strongly affect how the body processes drugs (known as CYP3A inhibitors or inducers) within 14 days before the first dose of the study drug (confirm with trial site if unsure which medications apply).
  • People who have taken certain medications that interact with specific drug transport proteins in the body (P-glycoprotein or BCRP inhibitors or inducers) within 14 days before the first dose of the study drug (confirm with trial site if unsure which medications apply).
  • People who have taken certain other medications that use the same drug transport pathways in the body within 14 days before the first dose of the study drug (confirm with trial site if unsure which medications apply).
  • People who still have unresolved or unstable serious side effects from previous chemotherapy or radiotherapy.
  • People who have had, or are scheduled to have, major surgery within 28 days before the first dose of the study drug.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Medical Director, Exscientia AI Ltd.

Phone: 385-374-1724

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Exscientia AI Ltd., a wholly owned subsidiary of Recursion Pharmaceuticals, Inc.
Registry
ClinicalTrials.gov
Start date
6 July 2023
Est. completion
1 January 2028

Where this trial is recruiting

🇧🇪 Belgium 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Number of Participants With Treatment Emergent Adverse Events (TEAEs); Phase 1: Number of Participants With Dose Limiting Toxicities (DLTs); Phase 2 : Objective Response Rate (ORR) as Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov