OncoMatch/Clinical Trials/NCT05719558
A Study of ASP1002 in Adults for Treatment of Solid Tumors
Is NCT05719558 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies ASP1002 for advanced solid tumors.
Treatment: ASP1002 — The main aims of this study are: * To check the safety of ASP1002 in people with certain solid tumors. * To check if the people can tolerate ASP1002. * To find a suitable dose of ASP1002. This study will be in 2 parts. In Part 1, different small groups of people will receive lower to higher doses of ASP1002. Any medical problems will be recorded at each dose. This is done to find suitable doses of ASP1002 to use in Part 2 of the study. In Part 2, other different small groups of people will receive doses of ASP1002 that worked the best in Part 1. People in this study will be adults with metastatic or locally advanced solid tumors with high levels of a protein called claudin 4. The people's cancer will have either spread to other parts of the body (metastatic) or spread to tissue close by (locally advanced). They will have been previously treated with available standard therapies or refused to receive those treatments. In both parts of the study, ASP1002 (the study treatment) will be given to people slowly through a tube into a vein. This is called an infusion. This will happen every week, every other week, or every 3 weeks, in treatment cycles. Treatment cycles may be 21 days or 28 days long. People in this study will continue treatment for up to 2 years until: they have medical problems that prevent them from continuing treatment; their cancer gets worse; they start other cancer treatment; they ask to stop treatment; they do not come back for treatment. During the study, people will visit the clinic several times for a health check. This includes standard safety checks and reporting any medical problems. Every few weeks, the study doctors will check if each person's cancer has stayed the same or got worse. This will be done by scans (CT or MRI scans). Tumor samples will be taken during the study and people will have the option of giving a tumor sample after treatment has finished. People will visit the clinic within 7 days after stopping treatment for a health check. Then, they may visit the clinic at 1 month and 3 months after stopping treatment for further health checks. People will have follow-up health checks for up to 1 year after their last dose of ASP1002.
Check if I qualifyExtracted eligibility criteria
Cancer type
Tumor Agnostic
Disease stage
Metastatic disease required
locally-advanced (unresectable) or metastatic solid tumor; at least 1 measurable lesion per RECIST v1.1
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Cannot have received: anti-cd137 therapy
Lab requirements
Blood counts
adequate organ function prior to start of study intervention
Kidney function
adequate organ function prior to start of study intervention
Liver function
adequate organ function prior to start of study intervention
Cardiac function
LVEF < 45% excluded; no recent MI/unstable angina; no significant cardiac arrhythmia or conduction block; QTcF > 470 ms excluded
Participant has adequate organ function prior to start of study intervention. Participant has had a myocardial infarction or unstable angina within 6 months prior to the start of study intervention or currently has an uncontrolled illness including, but not limited to, symptomatic congestive heart failure, clinically significant cardiac disease, unstable angina pectoris, cardiac arrhythmia, complete left bundle branch block, obligate use of a cardiac pacemaker, long QT syndrome or right bundle branch block with left anterior hemiblock (bifascicular block). Participant has a corrected corrected QT interval (QTcF) interval (single electrocardiogram (ECG)) > 470 ms within 7 days prior to the first study intervention administration on day 1. Participant has left ventricular ejection fraction (LVEF) < 45% noted in screening echocardiogram (ECHO).
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Yale University Cancer Center · New Haven, Connecticut
- Hartford HealthCare Cancer Institute at The Hospital of Central Connecticut · Plainville, Connecticut
- University of Florida · Gainesville, Florida
- University of Iowa Hospitals · Iowa City, Iowa
- Norton Cancer Institute · Louisville, Kentucky
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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