Clinical trial for Advanced Solid Tumors
Official title A Study of PHST001 in Advanced Solid Tumors
ClinicalTrials.gov ID: NCT06840886
What this study is testing
What is PHST001?
PHST001 is an investigational biological medicine being studied for advanced solid tumors.
Plain-language explanation of the investigational treatment. It is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- The study wants to learn how safe PHST001 is, how it behaves in the body, and whether it can shrink tumors when used alone or with other cancer drugs.
- Who it's for
- Adults who have advanced, relapsed, or resistant solid tumors such as ovarian, endometrial, breast, or brain cancers.
- What's involved
- Participants will receive PHST001 alone or with other cancer medicines, have regular clinic visits, blood tests, and scans to monitor safety and tumor response.
- Time commitment
- The study lasts several months, with frequent visits for dosing, monitoring, and testing as scheduled by the research team.
- Phase 1: an early, usually small safety study
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Histologically or cytologically confirmed advanced solid tumor which has relapsed from or been refractory to all locally available standard therapies.
- Adequate organ function per laboratory testing
- Pregnancy prevention requirements
- Measurable disease per RECIST v1.1 (or RANO) as assessed by the local site Investigator/radiology
- Performance status of 0 or 1 on Eastern Cooperative Oncology Group (ECOG) scale Key
You likely can't join if
- Diagnosis of immunodeficiency
- History of a previous additional malignancy, unless potentially curative treatment has been completed, with no evidence of malignancy for 2 years.
- Active known CNS metastases and/or carcinomatous meningitis from a systemic (non-CNS) primary malignancy.
- Received prior systemic anticancer therapy including investigational agents within 21 days or, if shorter, within 5 half-lives prior to the first...
- Prior autologous or allogeneic hematopoietic stem cell transplant or solid organ transplant.
- Received previous treatment with another agent targeting CD24.
The study team makes the final eligibility decision.
Where it is enrolling
- Beverly Hills, California, United States
- Los Angeles, California, United States
- Palo Alto, California, United States
- Denver, Colorado, United States
- New Haven, Connecticut, United States
- Chicago, Illinois, United States
- Boston, Massachusetts, United States
- Ann Arbor, Michigan, United States
- Grand Rapids, Michigan, United States
- Lake Success, New York, United States
- New York, New York, United States
- Durham, North Carolina, United States
- Nashville, Tennessee, United States
- Fort Worth, Texas, United States
- Houston, Texas, United States
- Irving, Texas, United States
- San Antonio, Texas, United States
- Fairfax, Virginia, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part, but confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
This study is enrolling now at Beverly Hills, California, United States; Los Angeles, California, United States; Palo Alto, California, United States; Denver, Colorado, United States; New Haven, Connecticut, United States; Chicago, Illinois, United States and 12 more locations. Enter your location above to see the nearest enrolling site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool that is independent of the study sponsor. Details come from ClinicalTrials.gov. The study team decides eligibility, and your own doctor gives medical advice.