A Study to Investigate the Pharmacokinetics and Safety of Subcutaneous Rilvegostomig in Adult Participants With Advanced Solid Tumors Previously Treated With Standard of Care Therapy

Recruiting now · Phase 1

Conditions studied: Advanced Solid Tumors

In brief

The purpose of this study is to determine the subcutaneous (SC) dose that gives rilvegostomig exposure comparable to the intravenous (IV) exposure, and to evaluate the pharmacokinetics (PK) and safety of SC rilvegostomig in adult participants with advanced solid tumors previously treated with standard of care therapy for whom immunooncology (IO) monotherapy would be deemed appropriate by the investigator.

Key facts

Study ID

NCT07161414

Run by

AstraZeneca

People needed

40

Starts

2025-11-25

Expected to finish

2029-07-24

Last updated by the study team

2026-07-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologically or cytologically documented advanced (metastatic and/or unresectable) solid tumor.
• Participants must have received prior anticancer treatment for the disease under study.
• IO monotherapy deemed appropriate by the investigator.
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 at enrollment with no deterioration.
• Minimum life expectancy of ≥ 12 weeks at enrollment.
• Adequate organ and marrow function.
• Body weight ≥ 30 kg.

You may not qualify if…

• Any severe or uncontrolled systemic diseases, which makes it undesirable for the participant to participate in the study or that would jeopardize compliance with the protocol.
• History of organ transplant.
• History of another primary malignancy that was active within past 2 years.
• Persistent toxicities caused by previous anticancer treatment(s) excluding alopecia, not yet improved to Grade ≤ 1 or baseline.
• Unstable, symptomatic brain metastasis or spinal cord compression.
• History of leptomeningeal carcinomatosis.
• Active primary immunodeficiency/active infectious disease including tuberculosis (TB), human immunodeficiency virus (HIV) infection or hepatitis A, B or C infection.
• History of clinically significant arrhythmia, cardiomyopathy of any etiology; symptomatic congestive heart failure, history of myocardial infarction within the past 6 months.
• Uncontrolled intercurrent illness including but not limited to ongoing or active known infection; interstitial lung disease (ILD), serious chronic gastrointestinal conditions associated with diarrhea; active non-infectious skin disease requiring systemic treatment.
• Active or prior documented autoimmune or inflammatory disorders requiring chronic treatment with steroids or other immunosuppressive treatment.
• Known allergy or hypersensitivity to rilvegostomig, hyaluronidase, or any excipients of the investigational products.
• Participants experienced a toxicity to prior immunotherapy that led to permanent discontinuation of prior immunotherapy.
• Prior anticancer treatment, including immunotherapy, up to 28 days prior to the first dose of study treatment.

Where it is running

• Research Site — Madrid, Spain (enrolling)
• Research Site — Fairfax, Virginia, United States (enrolling)
• Research Site — Huntersville, North Carolina, United States (enrolling)
• Research Site — Seoul, South Korea (enrolling)
• Research Site — Seoul, South Korea (enrolling)
• Research Site — San Antonio, Texas, United States (enrolling)
• Research Site — Barcelona, Spain (enrolling)
• Research Site — Madrid, Spain (enrolling)
• Research Site — Sutton, United Kingdom
• Research Site — Barcelona, Spain
• Research Site — Newcastle upon Tyne, United Kingdom

Full record on ClinicalTrials.gov

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