Phase 2 Pancreatic Cancer Trial, Recruiting NCT06962267 Sponsor: Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd. Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT06962267
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:

  • You are willing to take part and have signed a consent form agreeing to join the study
  • You are between 18 and 75 years old (at the time of signing the consent form)
  • You have been diagnosed with pancreatic ductal adenocarcinoma (a specific type of pancreatic cancer) confirmed by a tissue or cell sample — not a mixed type of pancreatic cancer
  • You have at least one tumor that can be measured on a scan, according to standard criteria
  • You have not had any previous systemic (whole-body) cancer treatments
  • You are in relatively good general health and able to carry out daily activities (with little or no limitation), and doctors expect you to live for more than 3 months
  • Your major organs (such as your heart, liver, and kidneys) are working well
  • If you could become pregnant, you must use reliable birth control during the study and for 6 months after it ends, have a negative pregnancy test within 7 days before joining, and must not be breastfeeding

Who may not be able to join:

  • You have had or currently have another type of cancer within the past 5 years — with some exceptions: certain fully treated cancers with no return, such as early-stage cervical cancer, skin basal cell carcinoma, certain nasopharyngeal cancers, or superficial bladder tumors may still be eligible (confirm with trial site)
  • You still have unresolved side effects (above a mild level) from any previous treatment, not counting hair loss
  • You have had major surgery, a serious injury, or have a wound or fracture that has not fully healed within the 28 days before starting the trial treatment
  • You have had a significant bleeding event within the 4 weeks before starting the trial treatment
  • You have had a serious blood clot event — such as a stroke, mini-stroke, deep vein thrombosis, or pulmonary embolism — within the past 6 months
  • You have hepatitis B and cannot receive regular antiviral treatment throughout the study, or you have hepatitis C and your condition is considered unstable or you need ongoing antiviral treatment that cannot be maintained during the study
  • You have active syphilis
  • You have a history of abusing mind-altering substances that you are unable to stop, or you have a mental health disorder
  • You have symptomatic interstitial lung disease or a condition that could increase the risk of lung damage from the study drug
  • You have any other severe or uncontrolled medical conditions
  • Scans show that your tumor has grown into or very close to major blood vessels, and your doctor believes there is a high risk of serious bleeding
  • You have cancer that has spread to the brain or the lining around the brain
  • You have fluid build-up around the lungs, heart, or in the abdomen that is not controlled and still requires repeated draining
  • You have had a severe allergic reaction to a large-molecule drug in the past, or are known to be allergic to any ingredient in the study drug (TQB2916)
  • You have been taking regular steroid medications or other immune-suppressing drugs at a significant dose within the past 28 days and will need to continue them after starting the trial (except for short-term use)
  • You have received a live attenuated vaccine (a type of vaccine made with a weakened live virus) within the 28 days before starting the study, or plan to receive one during the study
  • You have an active autoimmune disease that needed medical treatment within the 2 years before joining the study
  • You have taken part in another clinical trial for a cancer treatment within the 28 days before starting this study
  • Your doctor feels that other health conditions or circumstances make it unsafe or unsuitable for you to participate

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 2 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd.
Registry
ClinicalTrials.gov
Start date
18 April 2025
Est. completion
1 August 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

6-month progression-free survival rate

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: 2 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