Actively Recruiting
A Study of ASP2998 Given by Itself and Given With Standard Therapies in People With Solid Tumors
Led by Astellas Pharma Global Development, Inc. · Updated on 2026-04-23
428
Participants Needed
7
Research Sites
177 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Specific proteins found in tumors help the tumors spread and grow. People with solid tumors often have a protein called TROP2 in their tumor. ASP2998 is being developed to attach to TROP2 and then attack the tumor cells in people with solid tumors. ASP2998 will either be given by itself, or given together with one or more of standard cancer treatments pembrolizumab, carboplatin, and enfortumab vedotin. This is an early development study to collect information about ASP2998 in people with solid tumors. In this study ASP2998 will be given to humans for the first time. Early development studies are mostly about safety, but also to find the most suitable dose. Other aims are to check if ASP2998 shows signs of reducing tumor growth, to learn how the body processes ASP2998, and to check if there are changes either in the TROP2 protein or in the immune system. The main aim of the study is to check the safety of ASP2998 when given by itself and given with the standard cancer treatments, and how well it is tolerated. People in this study will be adults with locally advanced, unresectable or metastatic solid tumors. Locally advanced means the cancer has spread to nearby tissue. Unresectable means the cancer cannot be removed by surgery. Metastatic means the cancer has spread to other parts of the body. People's cancer came back or became worse after previous treatment or they couldn't receive treatment. Some people who had previously refused treatment may be able to take part. This will depend on which study treatment they receive. People will either have cancer in the bladder lining (urothelial cancer), non-small cell lung cancer (NSCLC), gastric cancer or cancer where the food pipe joins the stomach (gastroesophageal cancer, or GEJ), or certain types of breast cancer. People cannot take part if the cancer cells have spread to the thin tissue covering the brain and spinal cord (leptomeningeal disease), have symptoms of cancer in the brain or nervous system, or need medicines to suppress their immune system. In this study, ASP2998 will be given to humans for the first time. ASP2998 will either be given by itself, or given together with one or more of standard cancer treatments pembrolizumab, carboplatin and enfortumab vedotin. The standard cancer treatment given will depend on which cancer people have. The study will have 2 parts. In Part 1, different small groups of people will receive lower to higher doses of ASP2998 given by itself or together with one or more of the standard cancer treatments. Any medical problems will be recorded for each dose. This is done to find suitable doses of ASP2998 to use in Part 2. In Part 2, other different small groups will receive suitable doses of ASP2998 worked out from Part 1. ASP2998 will either be given by itself or given together with one or more of the standard cancer treatments. This part will also check how each type of cancer responds to ASP2998 when given by itself or together with the standard cancer treatments. In both parts of the study, safety checks will be done at each visit, and the doctors will continue to check for medical problems throughout the study. ASP2998 will be given slowly through a tube into a vein (infusion). People will continue to receive ASP2998 until their cancer gets worse, they can't tolerate ASP2998, they start other cancer treatment, they or the doctor decides the person should stop receiving ASP2998.
CONDITIONS
Official Title
A Study of ASP2998 Given by Itself and Given With Standard Therapies in People With Solid Tumors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults with confirmed locally advanced unresectable or metastatic solid tumors.
- Cancer types include urothelial carcinoma, non-small cell lung cancer (NSCLC), gastric/gastroesophageal junction (GEJ) cancer, or HER2-negative breast cancer.
- Participants must have progressed on, be ineligible for, or have refused all available standard therapies.
- Participants must have a life expectancy of at least 12 weeks.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- At least one measurable tumor lesion per RECIST v1.1.
- Adverse events from prior anticancer therapy must have improved to Grade 1 or baseline within 14 days prior to starting study treatment.
- Adequate organ function confirmed by laboratory tests.
- Females must not be pregnant or breastfeeding and must agree to contraception requirements.
- Males must agree to use contraception or abstain during treatment and for specified times after.
- Participants must agree not to participate in another interventional study while receiving study treatment.
You will not qualify if you...
- Weighing less than 40 kg at screening.
- Known active central nervous system (CNS) metastases, unless treated and stable without glucocorticoids.
- History of severe immune-related adverse events or toxicities from prior anticancer therapy not improved to Grade 1 or baseline.
- Active or prior autoimmune or inflammatory disorders requiring systemic immunosuppressive therapy within 3 years.
- Uncontrolled diabetes mellitus.
- Leptomeningeal disease.
- Additional malignancies requiring active treatment, with some exceptions for cured or remitted cancers.
- Recent systemic corticosteroid or immunosuppressive therapy within 14 days of study start.
- Active liver disease including hepatitis A, B, or C.
- Known HIV infection with AIDS-related complications.
- Significant cardiac disease or uncontrolled hypertension.
- History or current interstitial lung disease or pneumonitis.
- Poor pulmonary reserve or oxygen saturation below 92%.
- Requirement for chronic oxygen therapy.
- Recent major surgery within 4 weeks.
- Grade 2 or higher eye disorders.
- Significant bleeding risk or life-threatening bleeding history.
- Current peripheral neuropathy Grade 2 or higher (for certain cohorts).
- History of Grade 2 or higher hearing loss (for carboplatin cohorts).
- Prior treatment with TROP2 agents, STING agonists, or TopI inhibitors (with some exceptions).
- Prior anticancer therapy or investigational therapy within set washout periods.
- Recent radiation therapy within 14 days without recovery.
- Active infection requiring intravenous antibiotics.
- Expected need for other anticancer therapies during study.
- Use of anticoagulants or antiplatelet agents (except low dose aspirin).
- Hypersensitivity to study drugs or components.
- History of life-threatening allergic reactions to similar drug types.
AI-Screening
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Trial Site Locations
Total: 7 locations
1
John Theurer Cancer Center at Hackensack University Medical Center
Hackensack, New Jersey, United States, 07601
Actively Recruiting
2
START New York Long Island
New Hyde Park, New York, United States, 11042
Actively Recruiting
3
Tennessee Oncology
Nashville, Tennessee, United States, 37203
Actively Recruiting
4
NEXT Virginia
Fairfax, Virginia, United States, 22031
Actively Recruiting
5
National Cancer Center Hospital East
Kashiwa-shi, Chiba, Japan
Actively Recruiting
6
National Cancer Center Hospital
Chuo-ku, Tokyo, Japan
Actively Recruiting
7
The Cancer Institute Hospital of JFCR
Koto-ku, Tokyo, Japan
Actively Recruiting
Research Team
A
Astellas Pharma Global Development, Inc.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
TREATMENT
Number of Arms
6
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