drugset / Trial / NCT05419401

A Study to Investigate the Absolute Bioavailability, Absorption, Metabolism, Distribution and Excretion of [14C]AZD5363 (Capivasertib)

NCT05419401

Phase 1 Completed 7 enrolled AstraZeneca Quotient Sciences · collab
NaSequentialOpen-labelTreatment

Summary

The Sponsor is developing the test medicine, Capivasertib, for the potential treatment of primary breast and prostate cancer. This two-part healthy volunteer study will try to identify the absolute bioavailability (amount of the test medicine that enters the blood stream), mass balance recovery (how much radioactivity can be recovered from the urine and faeces) and the rates and routes of elimination of the test medicine.

Timeline

Start
2022-04-11
Primary completion
2022-07-12
Completion
2022-07-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Capivasertib Small molecule 100 ug Oral
Subject Capivasertib Small molecule 200 mg Oral
Subject Capivasertib Small molecule 400 mg Oral

Indications

No indication recorded.