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NCT01110226: 0805GCC
Trial Of Cisplatin And KML-001 in Platinum Responsive Malignancies
Phase 1 trial testing KML-001 in Non-Small Cell Lung Cancer, Small Cell Lung Cancer in 23 participants. Terminated before completion.
22 October 2015
Quick facts
| Lead sponsor | University of Maryland, Baltimore |
|---|---|
| Phase | Phase 1 |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 23 |
| Start date | 27 April 2010 |
| Primary completion | 22 October 2015 |
| Estimated completion | 27 October 2015 |
| Sites | 1 location across United States |
Drugs / interventions tested
Conditions studied
- Non-Small Cell Lung Cancer, Small Cell Lung Cancer — all drugs for Non-Small Cell Lung Cancer, Small Cell Lung Cancer →
- Platinum Responsive Malignancies — all drugs for Platinum Responsive Malignancies →
Sponsor
University of Maryland, Baltimore
Who can join
18 and older, any sex, with Non-Small Cell Lung Cancer, Small Cell Lung Cancer or Platinum Responsive Malignancies. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This is a Phase I Clinical Trial. Phase I studies are designed to determine the amount of investigational drugs that can be safely tolerated and to define the side effects that limit the dose. The drug administered in this study is KML-001. It is a highly soluble, orally available arsenic agent. It is currently being tested to determine its effects on telomerase activity. In other words, the purpose of this research study is to find the highest dose of KML001, that can be given without causing severe side effects when it is combined with a standard, commercially available anti-cancer drug called cisplatin.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Targeting Telomere Dynamics as an Effective Approach for the Development of Cancer Therapeutics.
Tao HY, Zhao CY, Wang Y, Sheng WJ, et al · · 2024 · cited 5× · PMID 38708177 · DOI 10.2147/ijn.s448556 -
Targeting pattern recognition receptors for cancer therapy: Mechanisms and strategies.
Ouyang D, Chen R, Xie H, Yang X, et al · · 2025 · cited 1× · PMID 41311391 · DOI 10.1016/j.apsb.2025.09.007
Verify or expand the search:
- PubMed search for NCT01110226
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other University of Maryland, Baltimore trials
Trials by the same sponsor.
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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 NCT01110226 (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 University of Maryland, Baltimore
- Last refreshed: 17 March 2020
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/NCT01110226.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing