Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

TQB2868 clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 4 trials in our China register that name TQB2868 as an intervention. Synced 9 Nov 2026
4Current trials
3Recruiting now
3Lead sponsors
1Country register
At a glance

TQB2868 is named as an intervention in 4 current clinical trials in our China register. 3 are recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is Fudan University (2). The most-studied condition is Breast Neoplasm.

Patient leaflets for TQB2868

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting375%
  • Not yet open125%

Trials by phase

  • Phase 2375%
  • Phase 3125%
01

Clinical trials of TQB2868

4 trials
StudyPhaseStatusLead sponsorRegisters
Clinical Trial Comparing TQB2868 Injection Combined With Anlotinib Hydrochloride Capsules With Placebo Combined With Chemotherapy as First-line Treatment for Metastatic Pancreatic Ductal Adenocarcinoma (mPDAC)
NCT07165951 · ClinicalTrials.gov ↗ · Metastatic Pancreatic Ductal Adenocarcinoma
Phase 3 Recruiting Shanghai Chia Tai Tianqing Pharmaceutical Technology Development Co., Ltd China
Fudan University Shanghai Cancer Center Breast Cancer Precision Platform Series Study- Neoadjuvant Therapy
NCT05582499 · ClinicalTrials.gov ↗ · Breast Neoplasm, Breast Cancer, Breast Tumors
Phase 2 Recruiting Fudan University China
Clinical Study of TQB2868 Injection Combined With Anlotinib Capsule and Chemotherapy in the First-line Treatment of Metastatic Pancreatic Neoplasms
NCT06767813 · ClinicalTrials.gov ↗ · Pancreatic Neoplasms
Phase 2 Recruiting Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd China
Cryoablation Combined With Anlotinib Plus TQB2868 in Patients With Advanced Intrahepatic Cholangiocarcinoma
NCT07846267 · ClinicalTrials.gov ↗ · Intrahepatic Cholangiocarcinoma
Phase 2 Not yet open Fudan University China

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with TQB2868

7 conditions
Breast Neoplasm1Breast Cancer1Breast Tumors1Triple-Negative Breast Cancer (TNBC)1Metastatic Pancreatic Ductal Adenocarcinoma1Pancreatic Neoplasms1Intrahepatic Cholangiocarcinoma1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Fudan University2
Shanghai Chia Tai Tianqing Pharmaceutical Technology Development Co., Ltd1
Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China43

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about TQB2868 trials

How many clinical trials are testing TQB2868?

4 current trials in our China register name TQB2868 as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are TQB2868 trials recruiting patients?

Yes. 3 of the 4 trials are recruiting: 3 with sites in China. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors TQB2868 clinical trials?

Fudan University (2), Shanghai Chia Tai Tianqing Pharmaceutical Technology Development Co., Ltd (1) and Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd (1). The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how TQB2868 works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how TQB2868 works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists TQB2868 (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 9 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.