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NCT02314884

A Phase I, Open-label, Dose-escalation Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-tumor Activity of Cafusertib Hydrochloride in Patients With Advanced Solid Tumors

Status unknown Phase 1 Last updated 10 December 2014
What this trial tests

Phase 1 trial testing Cafusertib Hydrochloride in Neoplasms in 40 participants. Status unknown.

Timeline
1 November 2014
Primary endpoint
1 December 2015
1 February 2016

Quick facts

Lead sponsorJiangsu Hansoh Pharmaceutical Co., Ltd.
PhasePhase 1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment40
Start date1 November 2014
Primary completion1 December 2015
Estimated completion1 February 2016
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Jiangsu Hansoh Pharmaceutical Co., Ltd. — full company profile →

Who can join

Adults 18 to 75, any sex, with Neoplasms. 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.

Sponsor's own description

A Phase I, Open-label, Dose-escalation Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-tumor Activity of Cafusertib Hydrochloride in Patients With Advanced Solid Tumors

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Neoplasms

Currently open trials in the same condition.

Other Jiangsu Hansoh Pharmaceutical Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT02314884.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing