CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 404 target
Drug / intervention
PM8002 +2 moredrug
Likely dose
Paclitaxel 175mg/m2from 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/NCT06616532
NCT06616532Phase 3ActiveOn Track

A Multicenter, Open-lable, Randomized Phase III Study of PM8002 in Combination With Paclitaxel Compared With Chemotherapy as Second-line Treatment in Small Cell Lung Cancer

Biotheus Inc.·interventional·Posted Sep 27, 2024·Updated May 22, 2026

In Brief

A Phase 3 clinical trial evaluating PM8002, Paclitaxel, and 1 other intervention for SCLC. Active but no longer recruiting, targeting 404 participants across 45 sites.

Detailed Summary

PM8002 is a bispecific antibody targeting PD-L1 and VEGF. This study will evaluate the efficacy and safety of PM8002 in combination with Paclitaxel as second-line treatment for SCLC

Study Details

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

Timeline

Phase 3Active
20252026202720282029
First PostedSep 27, 2024
Enrollment StartNov 13, 2024
Primary CompletionJan 25, 2027
Study CompletionDec 25, 2028
TodayJul 1, 2026
Enrollment to primary: 2.2 yearsPosted 1.8 years agoPrimary completion in 7 months

Interventions

PM8002drug

Following a predefined dose and date.

Paclitaxeldrug

175mg/m2 via IV infusion on Day 1 Q3W

Topotecandrug

1.25mg/m2/day via IV infusion on Days 1-5 Q3W