OncoMatch

OncoMatch/Clinical Trials/NCT06951997

QL1706 Plus Chidamide, AG as First-line Treatment for Metastatic Pancreatic Cancer

Is NCT06951997 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including QL1706 and Chidamide for metastatic pancreatic cancer.

Phase 2RecruitingTianjin Medical University Cancer Institute and HospitalNCT06951997Data as of Jun 2026Location: China

Treatment: QL1706 · Chidamide · Gemcitabine · Nab-paclitaxelThis is a single-center, open-label, exploratory study aims to assess the efficacy and safety of QL1706 plus nab-paclitaxel and gemcitabine as first-line treatment for patients with metastatic pancreatic adenocarcinoma.

Check if I qualify

Extracted eligibility criteria

Treatments studied

Targeted therapy

Chidamide

Chemotherapy

GemcitabineNab-paclitaxel

Other

QL1706

Cancer type

Pancreatic Cancer

Biomarker criteria

Excluded: BRCA1 germline mutation

Excluded: BRCA2 germline mutation

Disease stage

Required: Stage IV

Metastatic disease required

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: immune checkpoint inhibitor (anti-PD-1, anti-PD-L1, anti-CTLA-4)

Prior treatment with immune checkpoint inhibitors (e.g., anti-PD-1/PD-L1/CTLA-4 antibodies)

Cannot have received: immune checkpoint agonist (anti-ICOS, anti-CD40, anti-CD137, anti-GITR, anti-OX40)

immune checkpoint agonists (e.g., anti-ICOS/CD40/CD137/GITR/OX40 antibodies)

Cannot have received: immune cell therapy (CAR-T)

immune cell therapy (e.g., CAR-T)

Lab requirements

Blood counts

platelet count ≥90x10^9/l, white blood cell count ≥ 3.5 × 10⁹/l, absolute neutrophil count (anc) ≥1.5x10^9/l, hemoglobin > 90g/l

Kidney function

urea/urea nitrogen (bun) and creatinine (cr) ≤ 1.5 × uln (and creatinine clearance rate (ccr) ≥ 50 ml/min)

Liver function

ast and alt ≤ 2.5 times uln, total bilirubin ≤ 1.5 uln

Cardiac function

left ventricular ejection fraction (lvef) ≥ 50%, qtcf interval (fridericia correction) < 470 ms

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06951997 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Are patients with BRCA1 alterations eligible?

No. BRCA1 germline mutation is an exclusion criterion.

Are patients with BRCA2 alterations eligible?

No. BRCA2 germline mutation is an exclusion criterion.

What disease stage is eligible?

Stage IV is required (metastatic disease required).

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify