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NCT07002346: INVIGORATE

INVIGORATE: A Study of QL1706 and Bevacizumab in Advanced First-Line Ovarian Clear Cell Carcinoma

Not yet recruiting Phase 3 Last updated 3 June 2025
What this trial tests

Phase 3 trial testing QL1706 (bispecific antibody targeting PD-1 and CLTA-4) in Ovarian Clear Cell Carcinoma in 226 participants. Not yet recruiting.

Timeline
1 June 2025
Primary endpoint
1 June 2027
1 June 2029

Quick facts

Lead sponsorTongji Hospital
PhasePhase 3
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment226
Start date1 June 2025
Primary completion1 June 2027
Estimated completion1 June 2029
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Tongji Hospital

Who can join

Adults 18 to 75, female only, with Ovarian Clear Cell Carcinoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to learn if QL1706 combined with bevacizumab can effectively treat adult female patients (18 to \<75 years old) with newly diagnosed FIGO stage IC-IV advanced ovarian clear cell carcinoma. The main questions it aims to answer are: 1. Does QL1706 combined with bevacizumab, compared to platinum-based chemotherapy, prolong patients' progression-free survival (PFS)? 2. What is the safety profile of QL1706 combined with bevacizumab, such as what medical problems (adverse events) do participants experience? Researchers will compare QL1706 combined with bevacizumab (experimental arm) to a standard chemotherapy regimen of paclitaxel plus carboplatin (control arm) to see if QL1706 combined with bevacizumab is more effective in the first-line treatment of advanced ovarian clear cell carcinoma. Participants will: 1. Be randomly assigned to receive either QL1706 combined with bevacizumab (QL1706 administered every 3 weeks, bevacizumab administered every 3 weeks) or paclitaxel plus carboplatin chemotherapy (administered every 3 weeks). 2. Visit the research center regularly for drug infusions, medical examinations (such as vital signs, physical exams, laboratory tests), and tumor imaging assessments. 3. Complete quality of life questionnaires as required.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Advancements in the utilization of immune checkpoint inhibitors for the treatment of gynecological tumors.
    Su Z, Zhang X, Xu J, Shen Y. · · 2026 · PMID 41983132 · DOI 10.3389/fimmu.2026.1686568
  2. Advances in PD-1 and CTLA-4 dual-target immunotherapy for ovarian cancer.
    Li DM, Pei KG, Yu XZ, Qie MR, et al · · 2025 · PMID 41256843 · DOI 10.3389/fimmu.2025.1686532

Verify or expand the search:

Other trials of QL1706 (bispecific antibody targeting PD-1 and CLTA-4)

Trials testing the same drug.

Other recruiting trials for Ovarian Clear Cell Carcinoma

Currently open trials in the same condition.

Other Tongji Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07002346.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing