|

Study for AZD4360 in Participants With Advanced Solid Tumours

RECRUITINGPhase 1/2Sponsored by AstraZeneca
Actively Recruiting
PhasePhase 1/2
SponsorAstraZeneca
Started2025-04-29
Est. completion2027-03-31
Eligibility
Age18 Years – 130 Years
Healthy vol.Accepted
Locations3 sites

Summary

The purpose of this study is to evaluate the safety, tolerability, PK, immunogenicity, pharmacodynamics, and preliminary efficacy of AZD4360 in adult participants with locally advanced or metastatic solid tumours selected for expression of CLDN18.2.

Eligibility

Age: 18 Years – 130 YearsHealthy volunteers accepted
Inclusion Criteria:

1. Participant must be ≥ 18 at the time of signing the ICF.
2. Eastern cooperative oncology group performance status of 0-1 with no deterioration over the previous 2 weeks prior to baseline or day of first dosing.
3. Minimum life expectancy of 12 weeks in the opinion of the Investigator.

4 Adequate organ and marrow function, as defined by protocol.

5\. Contraceptive use by men or women should be consistent with local regulations, as defined by protocol.

6\. Histologically confirmed advanced or metastatic Pancreatic ductal adenocarcinoma (PDAC), Gastric or Gastroesophageal junction cancer (G/GEJC), and Biliary tract cancer (BTC) with documented positive CLDN18.2 expression.

7\. Participants must have received at least one prior line of systemic therapy in the advanced/metastatic disease.

8\. At least one measurable lesion according to RECIST v1.1.

Exclusion Criteria:

1. Human Epidermal Growth Factor Receptor 2 (HER2) positive (3+ by IHC or 2+ by IHC and positive by in situ hybridisation) or indeterminate G/GEJC participants.
2. Unstable or active peptic ulcer disease or digestive tract bleeding including but not limited to clinically significant bleeding in the setting of prior CLDN18.2 directed therapy.
3. Participants with clinically significant ascites that require drainage.
4. Central nervous system (CNS) metastases or CNS pathology, as defined by protocol.
5. With spinal cord compression or with high risk of paralysis.
6. History of non-infectious interstitial lung disease/pneumonitis.
7. Participant has cardiac abnormalities, as defined by protocol.
8. History of another primary malignancy within 2 years prior to screening.
9. Known serologic status reflecting active hepatitis B or hepatitis C.
10. Known HIV infection that is not well controlled.
11. Active tuberculosis infection.

Conditions5

Biliary Tract CancerCancerGastric CancerGastroesophageal-junction CancerPancreatic Ductal Adenocarcinoma

Locations3 sites

California

1 site
Research Site
Santa Monica, California, 90404

Rhode Island

1 site
Research Site
Providence, Rhode Island, 02903

Texas

1 site
Research Site
Houston, Texas, 77030

Browse More Trials

Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.