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A Study to Investigate Safety of AZD6750 in Adult Participants With Select Advanced or Metastatic Solid Tumors

NCT 07115043

Brief Summary

A Study to Investigate Safety of AZD6750 in Adult Participants With Select Advanced or Metastatic Solid Tumors.

Intervention / Treatment 

  • Drug: AZD6750
  • Drug: Rilvegostomig

Inclusion criteria:

  • Participant ≥ 18 year
  • ECOG PS of 0 to 1
  • Provision of ‘archival’ tumor specimen
  • At least one measurable lesion according to RECIST v1.1,
  • Minimum life expectancy of 12 weeks
  • Adequate and stable cardiac function
  • Adequate bone marrow, liver and kidney function
  • Body weight ≥ 35 kg
  • Capable of giving signed informed consent

Module 1 specific inclusion criteria:

• Participants with locally advanced or metastatic select solid tumors (MM, Squamous cell carcinoma of skin, MCC, NSCLC, Head and neck squamous cell carcinoma, Gastric cancer/gastroesophaegeal junction cancer, RCC, HGSOC, Triple negative breast cancer) who have received adequate SoC

Module 2 specific inclusion criteria:

  • Participants with Stage IV NSCLC Dose Escalation/Backfills
    1. Have received at least one prior regimen in metastatic setting (2L+ NSCLC). Participants with actionable tumor alterations should have received targeted therapy if locally available OR
    2. Have not received systemic therapy (1L NSCLC) and have PD-L1 expression ≥ 1%.

      Dose Expansion

    1. Have not received systemic therapy (1L NSCLC) and have PD-L1 expression ≥ 1%.

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