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NCT02688101

Dose-finding and Pharmacokinetic Study of DpC, Administered Orally to Patients With Advanced Solid Tumors

Completed Phase 1 Last updated 21 February 2019
What this trial tests

Phase 1 trial testing DpC in Neoplasms in 14 participants. Completed in 26 October 2017.

Timeline
11 April 2016
Primary endpoint
26 October 2017
26 October 2017

Quick facts

Lead sponsorCollaborative Medicinal Development Pty Limited
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment14
Start date11 April 2016
Primary completion26 October 2017
Estimated completion26 October 2017
Sites4 locations across Australia

Drugs / interventions tested

Conditions studied

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):

  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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:

Other recruiting trials for Neoplasms

Currently open trials in the same condition.

Other Collaborative Medicinal Development Pty Limited trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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