Clinical trial · Interventional
A Study of PLM60 in Subjects With Relapsed Small-cell Lung Cancer After Platinum-based First-Line Chemotherapy
An Open-label, Multi-center, Phase 2 Study of Liposome-entrapped Mitoxantrone Hydrochloride Injection (PLM60) in Subjects With Relapsed Small-cell Lung Cancer After Platinum-based First-Line Chemotherapy
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): The sponsor has adjusted its R\&D strategy.
Summary
Brief summary (as posted)
This is an open, multicenter phase II clinical study for PLM60. The primary aim of the study is to observe the initial efficacy of PLM60 in treatment of small cell lung cancer. The secondary aim is to explore the safety and PK characteristics of PLM60
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Small Cell Lung Cancer | Lung Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| PLM60 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Cohort A: PLM60
- description
- 20 mg/m2, 4 weeks/cycle, administered on day 1 of each cycle
- interventionNames
- Drug: PLM60
- type
- EXPERIMENTAL
- label
- Cohort B: PLM60
- description
- 15mg/m2, 3 weeks/cycle, administered on day 1 of each cycle
- interventionNames
- Drug: PLM60
Primary outcomes (1)
- measure
- Objective response rate (ORR)
- timeFrame
- Through study completion, an average of 2 year
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histologically confirmed diagnosis of SCLC; 2. Must have recurrence or progression after platinum-based first-line chemotherapy or chemoradiation therapy for the treatment of SCLC; 3. ECOG performance status 0\~2; 4. Measurable lesion according to RECIST v1.1; 5. Life expectancy ≥ 12 weeks; 6. Adequate organ function; 7. Signed informed consent from the patient. Exclusion Criteria: 1. Radical surgical treatment for primary small cell lung cancer; 2. Any anti-tumor treatment received within 4 weeks before the first use of the study drug; 3. Untreated or symptomatic central nervous system (CNS) metastases; 4. Uncontrolled pleural effusion, pericardial effusion, or ascites requiring repeated drainage; 5. History of serious systemic diseases; 6. History of serious autoimmune diseases; 7. Those receiving treatment of adriamycin or other anthracyclines previously, with the total cumulative adriamycin (or adriamycin-equivalent) dose of \>360 mg/m2.
References
Publications (0)
Data not yet available