A Study of TAK-188 in Adults With Advanced or Spreading Solid Tumors (NCT07205718)
An Open-label, Dose Escalation and Expansion, Phase 1/2 Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of TAK- 188, an Anti-CCR8 Antibody-Drug- Conjugate, as a Single Agent in Adult Participants With Locally Advanced or Metastatic Solid Tumors
๐ฉบ Plain-English Summary (8th-Grade Level)
TAK-188 is a new medicine that targets a protein called CCR8, which is found on the surface of certain cells (Tregs) inside tumors. These cells can weaken the body's ability to fight cancer. TAK-188 may help to remove these Tregs. Removing these Tregs may allow more cancer-fighting cells (CD8+ T cells) to attack the tumor and potentially stop tumors from growing. In this study, researchers want to learn if TAK-188 can help the body's immune system better fight cancer in adults with advanced cancers which have not gotten better with regular treatments. The main aims of this study are to check if TAK-188 is safe in adults with advanced or spreading (metastatic) solid tumors, if participants tolerate the treatment with TAK-188 and to learn if TAK-188 works well in adults with certain advanced cancers after their previous treatments didn't work. Participants may receive TAK-188 for up to 1 year. Their health will be monitored after the treatment has ended for up to another year.
Who can join: Review the eligibility criteria below.
Location: UCLA Health-Santa Monica Cancer Care (Cancer Care - Santa Monica) โ Santa Monica, California
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (15 Sites)
- UCLA Health-Santa Monica Cancer Care (Cancer Care - Santa Monica) โ Santa Monica, California
- Yale School of Medicine - Smilow Cancer Hospital - Center for Thoracic Cancers โ New Haven, Connecticut
- Florida Cancer Specialists - Lake Nona โ Orlando, Florida
- Johns Hopkins โ Baltimore, Maryland
- Barbara Ann Karmanos Cancer Institute โ Detroit, Michigan
- START Midwest โ Grand Rapids, Michigan
- Washington University โ St Louis, Missouri
- University Hospitals Cleveland Medical Center โ Cleveland, Ohio
- Providence Cancer Institute, Franz Clinic โ Portland, Oregon
- Fox Chase Cancer Center โ Philadelphia, Pennsylvania
- SCRI Oncology โ Nashville, Tennessee
- MD Anderson Cancer Center โ Houston, Texas
- NEXT Dallas โ Irving, Texas
- START San Antonio โ San Antonio, Texas
- NEXT Virginia โ Fairfax, Virginia
๐ Contact the Study Coordinator
Phone: (877) 825-3327
Email: medinfoUS@takeda.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Advanced or Metastatic Solid Tumors
- A Study of MK-1484 as Monotherapy and in Combination With Pembrolizumab (MK-3475) In Advanced or Metastatic Solid Tumors (MK-1484-001) โ Sioux Falls, South Dakota
- A Study of ERAS-007 as Monotherapy or in Combination With ERAS-601 in Patients With Advanced or Metastatic Solid Tumors โ Denver, Colorado
- A Study to Assess Naporafenib (ERAS-254) Administered With Trametinib in Patients With RAS Q61X Mutations โ San Francisco, California
- Safety and Tolerability of IPH4502 in Patients With Advanced Solid Tumors โ Boston, Massachusetts
- A Dose Escalation/Expansion Study of ERAS-601 in Patients With Advanced or Metastatic Solid Tumors โ Birmingham, Alabama
- A Dose Escalation and Expansion Study of TAC-001 in Patients With Select Advanced or Metastatic Solid Tumors โ Los Angeles, California
Explore by condition: All Advanced or Metastatic Solid Tumors clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.