Conversion Therapy

3

Review clinical trials related to Conversion Therapy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Ipilimumab N01 Combined With Sintilimab, Bevacizumab Biosimilar, and Hepatic Arterial Infusion Chemotherapy as Conversion Therapy for Unresectable Intermediate-Advanced Hepatocellular Carcinoma

Conversion therapy for unresectable intermediate-advanced hepatocellular carcinoma (uHCC) has evolved from systemic therapy to combined local-systemic approaches, but current regimens still have limited surgical conversion rates. This prospective, single-arm phase II study evaluates a combination regimen of PD-1 inhibitor (sintilimab) plus CTLA-4 inhibitor (ipilimumab N01), bevacizumab biosimilar, and HAIC for patients with initially unresectable intermediate-advanced HCC. The primary goal is to achieve a higher surgical conversion rate with manageable safety

Participants needed: 43
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Tianjin Medical University Cancer Institute and HospitalUpdated: May 1, 2026Locations: 1
Eligibility criteria

Written informed consent must be signed prior to initiation of any study-related... [+18]

Fibrolamellar HCC, sarcomatoid HCC, or combined hepatocellular-cholangiocarcinom... [+32]

Status: Not yet recruiting

Tislelizumab Plus Chemotherapy and BACE for Unresectable NSCLC

The goal of this phase 2 trial is to evaluate the efficacy and safety of tislelizumab combined with intravenous chemotherapy and bronchial artery chemoembolization (BACE) as conversion therapy for patients with initially unresectable stage IIIA-IIIB non-small cell lung cancer (NSCLC). The main questions it aims to answer are: * What is the 1-year event-free survival (EFS) rate with this treatment? * Can this treatment improve tumor response and the chance of curative-intent resection? * What adverse events occur during treatment? Participants will receive tislelizumab, intravenous chemotherapy, and BACE for up to 4 cycles. Tumor response and resectability will be evaluated by imaging and multidisciplinary team (MDT) assessment every 2 cycles. Participants who become resectable may undergo surgery followed by postoperative treatment per protocol. Participants who remain unresectable after 4 cycles will receive guideline-recommended chemoradiotherapy followed by tislelizumab consolidation. Regular follow-up will be performed for efficacy and safety assessment.

Participants needed: 39
Trial details
Phase: Phase 2Age: 18-80Biological sex: AllType: InterventionalSponsor: Sichuan Cancer Hospital and Research InstituteUpdated: May 1, 2026Locations: 1
Eligibility criteria

Age 18 to 80 years [+12]

Prior local therapy for NSCLC, including radiotherapy or interventional therapy [+12]

Status: Not yet recruiting

A Randomized Trial of Surgical Decision-Making Guided by TDTP-RECIST

This project aims to conduct a prospective, multicenter, randomized controlled clinical trial. The study plans to enroll 270 patients with locally advanced iCCA who have successfully undergone GOLP conversion therapy. Participants will be randomized at a 1:2:2 ratio into three arms: Control Arm (continued medication), Direct Surgery Arm, and TDTP-RECIST Assessment Arm. The primary endpoint is Overall Survival (OS).

Participants needed: 270
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Shanghai Zhongshan HospitalUpdated: Oct 6, 2025Locations: 1
Eligibility criteria

Male or female aged 18-75 years; [+6]

Pathologically diagnosed hepatocellular carcinoma, combined hepatocellular-chola... [+7]