๐๏ธ Verified NIH Record โข Updated 2024-11-13
A Phase 1/2a Study of 23ME-00610 in Patients With Advanced Solid Malignancies (NCT05199272)
A Phase 1/2a, Multicenter, Open-Label, Dose-Escalation and Expansion Study of Intravenously Administered 23ME-00610 in Patients With Advanced Solid Malignancies
๐ต Active, Not Recruiting Phase1 / Phase2 ๐ Investigational Drug / Biologic Sponsor: 23andMe, Inc.
๐ฉบ Plain-English Summary (8th-Grade Level)
This is a first-in-human open-label Phase 1/2a study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary clinical activity of 23ME-00610 given by intravenous infusion in patients with advanced solid malignancies who have progressed on all available standard therapies
Who can join: Review the eligibility criteria below.
Location: Stanford Cancer Institute โ Palo Alto, California
Age range: 12 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 (13 Sites)
- Stanford Cancer Institute โ Palo Alto, California
- Emory University โ Atlanta, Georgia
- Karmanos Cancer Institute โ Detroit, Michigan
- R.J.Zuckerberg Cancer Center โ Lake Success, New York
- Cohen Children's Medical Center โ New Hyde Park, New York
- Oregon Health & Science University โ Portland, Oregon
- Vanderbilt University โ Nashville, Tennessee
- MD Anderson Cancer Center โ Houston, Texas
- START Center for Cancer Care โ San Antonio, Texas
- Virginia Cancer Specialists โ Fairfax, Virginia
- Ottawa Hospital Cancer Centre โ Ottawa, Ontario
- Princess Margaret Cancer Centre โ Toronto, Ontario
- The Hospital for Sick Children โ Toronto, Ontario
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.
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- A Study of AZD1390 and Stereotactic Body Radiotherapy (SBRT) for People With Metastatic Solid Tumor Cancer โ Middletown, New Jersey
- A Study of RP-3500 in Combination With Standard Radiation Therapy in People With Solid Tumor Cancer โ Basking Ridge, New Jersey
- Study of PD1 Blockade by Pembrolizumab With Stereotactic Body Radiotherapy in Advanced Solid Tumors โ Chicago, Illinois
- A Study Evaluating DS-1055a in Participants With Relapsed or Refractory Locally Advanced or Metastatic Solid Tumors โ New York, New York
- Concurrent Azeliragon With Craniospinal Irradiation โ New York, New York
Explore by condition: All Solid Tumor clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.