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Real-world study of Iparomlimab and Tuvonralimab (QL1706)-based therapy for gastrointestinal tumors

Real-world study of Iparomlimab and Tuvonralimab (QL1706)-based therapy for gastrointestinal tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121037
Enrollment
Unknown
Registered
2026-03-24
Start date
2026-03-25
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

gastrointestinal tumors

Interventions

Observation group:none

Sponsors

Nantong Tumor Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients with gastrointestinal tumors confirmed by pathology or cytology; 2.Age >=18 years, no gender restriction; 3.ECOG performance status 0–2; 4.Deemed eligible by the investigator to receive QL1706-based combination therapy; 5.Patients voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: 1.Confirmed pregnancy or breastfeeding; 2.Other conditions that, in the investigator’s judgment, make the patient unsuitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
safety(Including the occurrence of all adverse events during the treatment period, especially those related to the immune system.);

Secondary

MeasureTime frame
Progression-free survival;Disease control rate;Objective response rate;Overall survival;

Countries

China

Contacts

Public ContactLei Yang

Nantong Tumor Hospital

leiyang.53@163.com+86 158 5139 8092

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 4, 2026