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NCT07391670: IMFINZI-subQ

A Phase I Dose Escalation and Dose Expansion Study to Investigate the Pharmacokinetics and Safety of Subcutaneous Durvalumab

Recruiting now Phase 1 Last updated 17 April 2026
What this trial tests

Phase 1 trial testing SC durvalumab + rHu in Solid Tumours in 40 participants. Currently enrolling.

Timeline
31 March 2026
Primary endpoint
30 August 2027
30 August 2027

Quick facts

Lead sponsorAstraZeneca
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment40
Start date31 March 2026
Primary completion30 August 2027
Estimated completion30 August 2027
Sites19 locations across Georgia, Taiwan, Poland, South Korea, Australia

Drugs / interventions tested

Conditions studied

Sponsor

AstraZeneca — full company profile →

Who can join

18 and older, any sex, with Solid Tumours. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of the study is to determine a subcutaneous (SC: under the skin) durvalumab + recombinant human hyaluronidase (rHu) dose that yields systemic drug exposure similar to intravenous (IV: into the veins) durvalumab administration and to evaluate the pharmacokinetics and safety of SC durvalumab + rHu injection in participants with different types of solid tumours (cancers).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Solid Tumours

Currently open trials in the same condition.

Other AstraZeneca trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07391670.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing