Phase 2 Pancreatic Cancer Trial, Recruiting NCT03579836 Sponsor: BeyondBio Inc. Condition: Pancreatic Cancer
Back to Pancreatic Cancer

Phase 2 Pancreatic Cancer Trial, Recruiting

NCT03579836
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 have been diagnosed with pancreatic ductal adenocarcinoma or undifferentiated carcinoma of the pancreas, confirmed through a tissue or cell sample
  • People who have at least one tumour that can be measured using standard imaging guidelines (RECIST v1.1)
  • People whose general health and ability to carry out daily activities falls within a certain range on a standard scale (ECOG score of 0, 1, or 2 — confirm with trial site)
  • People with a life expectancy of more than 12 weeks
  • People whose bone marrow, kidneys, and liver are functioning adequately at the time of screening

Who may not be able to join:

  • People who have previously received treatment for locally advanced or metastatic pancreatic cancer
  • People who have had major surgery recently at the time of screening (confirm with trial site for timeframe)
  • People with brain metastases (cancer that has spread to the brain) that are not well controlled
  • People with an active bacterial infection
  • People who have or have had another type of cancer, other than certain skin cancers (basal cell carcinoma), early-stage cervical cancer (carcinoma in situ), or papillary thyroid cancer
  • People who are pregnant, planning to become pregnant, or breastfeeding
  • People with HIV, or active hepatitis B or C infection
  • People who have had a severe allergic reaction to either BEY1107 or Gemcitabine (the study drugs)

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 15 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

Phone: +82-42-716-0020

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
BeyondBio Inc.
Registry
ClinicalTrials.gov
Start date
14 May 2018
Est. completion
30 November 2026

Where this trial is recruiting

🇰🇷 South Korea

Primary endpoints

MTD & Safety assessment (Phase I); DCR(Disease Control Rate) in combination therapy of BEY1107 and Gemcitabine (Phase II)

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: 15 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