NCT07282262RecruitingPhase 2
An Exploratory Study on the Use of Ivosidenib for the Precise Treatment of Advanced Biliary Tract Malignancies With IDH1 Mutations in the Later Line of Therapy.
Source: ClinicalTrials.gov · Last updated 15 Dec 2025
Brief summary (registry, in English)
This is a multicenter, non-randomized, umbrella, open-label phase II clinical study, aiming to observe and evaluate, as well as explore the efficacy and safety of precision targeted therapy based on NGS technology for IDH1-mutated patients, specifically the combination of ivosidenib with multi-target tyrosine kinase inhibitors represented by lenvatinib or PD-1/PD-L1 in advanced biliary tract cancer patients who have failed systemic chemotherapy.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 300 (estimated)
- First submitted
- 2 Dec 2025
- Start date
- 1 May 2024
- Primary completion date
- 1 Oct 2026
- Lead sponsor
- Peking Union Medical College Hospital
- Diseases
- Liver and biliary tract cancer
- NCT number
- NCT07282262
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 300
- From 1 May 2024 to the primary completion date, 1 Oct 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Prior Treatment: Previous treatment with Ivosidenib.
- Recent Therapy: Local anti-tumor therapy or major surgery within 4 weeks prior to initiation.
- Concurrent Participation: Participation in another interventional clinical trial.
Other illness
- Cancer Type: Ampulla of Vater cancer.
- Allergy: Known hypersensitivity to any component of the study drugs.
- Medical Conditions:
- Uncontrolled hypertension.
- Significant cardiovascular disease.
- Active autoimmune disease.
- Uncontrolled active infection (e.g., HBV, HCV, HIV).
- Significant bleeding tendency or history.
- History of organ transplantation.
Other
- Pregnancy: Pregnant or breastfeeding women.
- Active or untreated CNS metastases.
- Severe non-healing wounds.
Who the study is looking for
- Voluntary Participation: Signed informed consent.
- Genetic Mutation: Presence of an IDH1 mutation confirmed by genetic testing.
- Disease Status:
- Newly diagnosed, untreated advanced/metastatic disease; OR
- Recurrence \>6 months after curative-intent surgery (with or without adjuvant therapy).
- Measurable Disease: At least one measurable lesion per RECIST 1.1.
- Performance Status: ECOG performance status of 0 or 1.
- Life Expectancy: ≥3 months.
- Organ Function: Adequate hematological, hepatic, and renal function.
- Contraception: Use of highly effective contraception for women of childbearing potential and men.
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Beijing Peking Union Medical College Hospital Outpatient Department Coordinator of this site? Confirm its status | Beijing | China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.