Early Phase 1 Pancreatic Cancer Trial, Recruiting NCT06577532 Sponsor: Ruijin Hospital Condition: Pancreatic Cancer
Back to Pancreatic Cancer

Early Phase 1 Pancreatic Cancer Trial, Recruiting

NCT06577532
Recruiting Early Phase 1

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:

  • You must be 18 years of age or older at the time of signing the consent form
  • You have been diagnosed with an advanced solid tumor (such as pancreatic cancer or non-small cell lung cancer) that has been confirmed by a tissue or cell sample, and your cancer has gotten worse or you could not tolerate at least one previous treatment — in some cases, people who have not yet had any treatment may also be considered if the doctor believes they could benefit
  • Your tumor must have a specific type of gene change (mutation) in a gene called KRAS that the trial is targeting
  • You must be well enough to carry out basic daily activities, based on a standard health scoring system rated 0 to 2 (confirm with trial site)
  • Doctors expect you to live for at least 12 weeks
  • Your liver, kidneys, and other major organs must be working well enough (confirm with trial site for specific requirements)

Who may not be able to join:

  • You have had another cancer in the past 5 years, unless it was a cured skin cancer (basal cell), a very early-stage bladder cancer, or a pre-cancerous condition of the breast or cervix
  • You have previously received a KRAS cancer vaccine
  • You have needed immune-suppressing or immune-modifying medications within 4 weeks before starting the trial, or you have a condition — including a history of organ transplant — that requires you to take such medications
  • You have a known allergy to any ingredient in the study drug
  • You have an uncontrolled infection in your body, or you have active tuberculosis (TB)
  • You have serious heart or blood vessel disease
  • You have brain metastases (cancer that has spread to the brain) that are causing symptoms or still need treatment — people with brain metastases that are not causing symptoms and do not need treatment may still be eligible
  • You have an active autoimmune or inflammatory disease (where your immune system attacks your own body)
  • You have a history of severe allergic reactions, uncontrolled eczema, or uncontrolled asthma
  • You have other serious medical conditions (confirm with trial site for details)
  • You have previously had an organ transplant, bone marrow transplant, or stem cell transplant

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 16 July 2026
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

Contact this trial

Principal Investigator: Baiyong Shen, Ruijin Hospital

Phone: 18817821319

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
Early Phase 1
Sponsor
Registry
ClinicalTrials.gov
Start date
24 September 2024
Est. completion
1 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Part I: The incidence and nature of dose-limiting toxicity (DLT) for ABO2102 as monotherapy or in combination with toripalilmab.; Part I: The incidence and severity of treatment-emergent adverse events (TEAE)s.; Part I: The incidence and severity of serious TEAEs (TESAE)s.; Part I: The incidence and severity of TEAEs leading to interruption or early termination of study treatment.; Part II: Overall Response Rate (ORR) per 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: 16 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