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Study details
Enrolling now

Study of AZD5863 for Advanced Solid Tumors

AstraZeneca
NCT IDNCT06005493ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

280

Study length

about 3.9 years

Ages

18+

Locations

3 sites in FL, MN, NY

What this study is about

This trial is testing a new treatment called AZD5863 in adults with advanced or metastatic solid tumors. The goal is to see if this medication is safe, well-tolerated, and effective against cancer.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take AZD5863

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Objective Response Rate (ORR), The number of patients with adverse events, The number of patients with adverse events of special interest, The number of patients with dose-limiting toxicity (DLT), as defined in the protocol., The number of patients with serious adverse events

Secondary: Disease Control Rate (DCR), Duration of response (DoR), Objective Response Rate (ORR), Overall Survival (OS), Pharmacokinetics of AZD5863: Area Under the concentration-time curve (AUC), Pharmacokinetics of AZD5863: Clearance, Pharmacokinetics of AZD5863: Maximum plasma concentration of the study drug (Cmax), Pharmacokinetics of AZD5863: Terminal elimination half-life (t 1/2)