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NCT00826644: COMBAT
A Randomized Prospective Multicenter Trial of Belotecan/Cisplatin Versus Etoposide/Cisplatin in Patients With Previously Untreated, Extensive-stage Small-cell Lung Cancer
Phase 3 trial testing Belotecan in Carcinoma, Small Cell in 147 participants. Completed in 1 February 2013.
1 February 2013
Quick facts
| Lead sponsor | Chonnam National University Hospital |
|---|---|
| Phase | Phase 3 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 147 |
| Start date | 1 January 2009 |
| Primary completion | 1 February 2013 |
| Estimated completion | 1 February 2013 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- Belotecan (BELOTECAN) — full drug profile →
- Etoposide (etoposide) — full drug profile →
- Cisplatin (cisplatin) — full drug profile →
Conditions studied
- Carcinoma, Small Cell — all drugs for Carcinoma, Small Cell →
Sponsor
Chonnam National University Hospital
Who can join
Adults 19 to 80, any sex, with Carcinoma, Small Cell. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
To assess the response Rate of Belotecan/Cisplatin versus Etoposide/Cisplatin in patients with previously untreated, extensive-stage small cell lung cancer
Time frame: two years
Sponsor's own description
Belotecan (Camtobell, CKD-602, Chong Kun Dang Pharm., Korea) is a new camptothecin derivative, that exhibits anticancer effects by inhibiting topoisomerase I. The investigators will have a randomized prospective multicenter trial of Belotecan/Cisplatin versus Etoposide/Cisplatin in patients with previously untreated, extensive-stage small cell lung cancer. Primary endpoints * to assess Response Rate Secondary endpoints * to assess Overall response duration, Time to progression, Overall survival
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
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A novel mutation panel for predicting etoposide resistance in small-cell lung cancer.
Qiu Z, Lin A, Li K, Lin W, et al · · 2019 · cited 45× · PMID 31417239 · DOI 10.2147/dddt.s205633 -
Belotecan/cisplatin versus etoposide/cisplatin in previously untreated patients with extensive-stage small cell lung carcinoma: a multi-center randomized phase III trial.
Oh IJ, Kim KS, Park CK, Kim YC, et al · · 2016 · cited 13× · PMID 27566413 · DOI 10.1186/s12885-016-2741-z
Verify or expand the search:
- PubMed search for NCT00826644
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Carcinoma, Small Cell
Currently open trials in the same condition.
- NCT04660929 — CAR-macrophages for the Treatment of HER2 Overexpressing Solid Tumors · Phase 1 · active not recruiting
Other Chonnam National University Hospital trials
Trials by the same sponsor.
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- NCT06227754 — OCT Versus Angiography for Culprit Lesion Revascularization in Acute Myocardial Infarction PatiEnts · NA · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00826644 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Chonnam National University Hospital
- Last refreshed: 2 August 2021
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00826644.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing