About this trial

This research study is studying a new compound, AZD8205, as a possible treatment for advanced or metastatic solid tumours alone or in combination with anti-cancer agents

Eligibility criteria

Qualifiers

Age ≥ 18 years

Relapsed/metastatic solid tumors treated with prior adequate standard of care therapy for tumor type and stage of disease or where in the opinion of the Investigator, a clinical trial is the best option for the next treatment based on response and/or tolerability to prior therapy.

Measurable disease per RECIST v1.1

Eastern Cooperative Oncology Group (ECOG) Performance Status: 0-1

Disqualifiers

Nitrosourea or mitomycin C within 6 weeks prior to the first dose of study treatment

Any investigational agents or study drugs from a previous clinical study within 5 half-lives or 28 days (whichever is shorter) prior to the first dose of study treatment

Cytotoxic treatment: 21 days

Non-cytotoxic drugs: 21 days or 5 half-lives (whichever is shorter)

Trial design

Treatments tested in this trial

  • AZD8205
  • AZD8205 and AZD2936 (Rilvegostomig)
  • AZD8205 and AZD5305 (saruparib)
  • AZD8205 and AZD5305 (saruparib) and AZD2936 (rilvegostomig)
  • AZD8205 in combination with AZD9574
  • AZD8205 in combination with AZD9574 plus rilvegostomig (AZD2936)

Treatment groups

460 Participants
are divided into 4 treatment groups

Locations

67
Australia
Research Site3168, Clayton Australia
Research SiteVIC 3000, Melbourne Australia
Research Site6009, Nedlands Australia
Belgium
Research Site1070, Anderlecht Belgium

Sponsors and collaborators

AstraZeneca

Lead sponsor