CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 10 target
Drug / intervention
LTC004+Toripalimabdrug
Likely dose
LTC004+Toripalimab 90μgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06490068
NCT06490068Phase 2RecruitingMonitorUpdated 23mo ago · Completion was 3mo ago
Slow Enrollment
Monitor

An Open, Single-arm, Phase II Clinical Study to Evaluate the Efficacy and Safety of LTC004 in Combination With Toripalimab in Patients With Advanced Solid Tumors Resistant to First-line Immunotherapy

Cancer Institute and Hospital, Chinese Academy of Medical Sciences·interventional·Posted Jul 8, 2024·Updated Jul 8, 2024

In Brief

A Phase 2 clinical trial evaluating LTC004+Toripalimab for Advanced Solid Tumor. Currently recruiting, targeting 10 participants across 1 site.

Signals

Enrolling slower than its timeline implies

Detailed Summary

To evaluate the efficacy and safety of LTC004 in combination with Toripalimab in 10 patients with advanced solid tumors resistant to first-line immunotherapy, all eligible subjects will receive LTC004 on day 1 of Week 1 and day 1 of week 3. Beginning at week 5, all subjects will receive LTC004 in combination with Toripalimab regimen until disease progression, intolerance, informed withdrawal or up to 2 years of dosing, whichever occurred first.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 2RecruitingOverdue
20252026
First PostedJul 8, 2024
Enrollment StartJun 4, 2024
Primary CompletionMar 31, 2026
TodayJul 1, 2026
Enrollment to primary: 1.8 yearsPosted 2.0 years ago

Interventions

LTC004+Toripalimabdrug

LTC004 on D1 of Week 1 and D1 of week 3. IV,90μg/kg. Beginning at week 5, all subjects will receive LTC004 in combination with Toripalimab. LTC004:D3,iv,45μg/kg,Q3W. Toripalimab:D1,iv,240mg,Q3W.