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NCT02688101
Dose-finding and Pharmacokinetic Study of DpC, Administered Orally to Patients With Advanced Solid Tumors
Phase 1 trial testing DpC in Neoplasms in 14 participants. Completed in 26 October 2017.
26 October 2017
Quick facts
| Lead sponsor | Collaborative Medicinal Development Pty Limited |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 14 |
| Start date | 11 April 2016 |
| Primary completion | 26 October 2017 |
| Estimated completion | 26 October 2017 |
| Sites | 4 locations across Australia |
Drugs / interventions tested
- DpC — full drug profile →
Conditions studied
- Neoplasms — all drugs for Neoplasms →
Sponsor
Collaborative Medicinal Development Pty Limited — full company profile →
Who can join
18 and older, any sex, with Neoplasms. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Multicenter, open-label, dose-escalation and pharmacokinetic study.
Publications & conference data
8 peer-reviewed publications reference this trial (live from Europe PMC):
-
Metallodrugs are unique: opportunities and challenges of discovery and development.
Anthony EJ, Bolitho EM, Bridgewater HE, Carter OWL, et al · · 2020 · cited 372× · PMID 34123239 · DOI 10.1039/d0sc04082g -
Iron and Cancer.
Torti SV, Manz DH, Paul BT, Blanchette-Farra N, et al · · 2018 · cited 335× · PMID 30130469 · DOI 10.1146/annurev-nutr-082117-051732 -
Targeting iron metabolism in drug discovery and delivery.
Crielaard BJ, Lammers T, Rivella S. · · 2017 · cited 279× · PMID 28154410 · DOI 10.1038/nrd.2016.248 -
Iron as a Central Player and Promising Target in Cancer Progression.
Jung M, Mertens C, Tomat E, Brüne B. · · 2019 · cited 195× · PMID 30641920 · DOI 10.3390/ijms20020273 -
Iron metabolism: pathophysiology and pharmacology.
Roemhild K, von Maltzahn F, Weiskirchen R, Knüchel R, et al · · 2021 · cited 193× · PMID 34090703 · DOI 10.1016/j.tips.2021.05.001 -
Modulation of Intracellular Copper Levels as the Mechanism of Action of Anticancer Copper Complexes: Clinical Relevance.
Babak MV, Ahn D. · · 2021 · cited 125× · PMID 34440056 · DOI 10.3390/biomedicines9080852 -
A mechanism for overcoming P-glycoprotein-mediated drug resistance: novel combination therapy that releases stored doxorubicin from lysosomes via lysosomal permeabilization using Dp44mT or DpC.
Seebacher NA, Richardson DR, Richardson DR, Jansson PJ. · · 2016 · cited 81× · PMID 27906178 · DOI 10.1038/cddis.2016.381 -
The novel thiosemicarbazone, di-2-pyridylketone 4-cyclohexyl-4-methyl-3-thiosemicarbazone (DpC), inhibits neuroblastoma growth in vitro and in vivo via multiple mechanisms.
Guo ZL, Richardson DR, Richardson DR, Kalinowski DS, et al · · 2016 · cited 77× · PMID 27678372 · DOI 10.1186/s13045-016-0330-x
Verify or expand the search:
- PubMed search for NCT02688101
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Collaborative Medicinal Development Pty Limited 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 NCT02688101 (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 Collaborative Medicinal Development Pty Limited
- Last refreshed: 21 February 2019
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/NCT02688101.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing