This multicentre, open-label, Phase 1b/2 study is designed as a 2 part study consisting of a dose-escalation, safety run-in Part A and a dose-expansion Part B
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Part A: Danvatirsen With Durvalumab MTDs (Maximum Tolerated Dose) or Recommended Doses for Dose-expansion
Timeframe: 35 days
Part A: AZD5069 With Durvalumab MTDs (Maximum Tolerated Dose) or Recommended Doses for Dose-expansion
Timeframe: 35 days
Part A: Safety and Tolerability in Terms of Adverse Events
Timeframe: At every treatment and follow up visit until disease progression, an average of 1 year.
Part B: ORR (Objective Response Rate) in Patients With IL/2L RM-SCCHN.
Timeframe: Assessed at every even-numbered cycles with RECIST until disease progression, up to 12 months.