Clinical trial for Ovarian Cancer
Official title Investigation of Ubamatamab Combination Therapy in Adult Participants With Platinum-Resistant Ovarian Cancer
ClinicalTrials.gov ID: NCT06787612
What this study is testing
What is Ubamatamab?
Ubamatamab is an investigational medicine, being studied as a potential treatment for ovarian cancer.
Also referred to as REGN4018.
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 if ubamatamab is safe, tolerable, and shows any anti‑cancer activity, both by itself and when combined with other cancer medicines. It also checks side effects, drug levels in the blood, and whether the body makes antibodies against it.
- Who it's for
- Adults whose ovarian, fallopian tube, or primary peritoneal cancer no longer responds to platinum‑based chemotherapy.
- What's involved
- Participants receive ubamatamab alone or together with bevacizumab, cemiplimab, fianlimab, REGN10597, and pegylated liposomal doxorubicin, plus regular safety labs and blood draws to measure drug levels and antibodies.
- Time commitment
- The trial lasts several months, with multiple clinic visits for infusions and tests according to the study schedule.
- Phase 2: a mid-size study of how well it works
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, women only
You may be able to join if
- Participants with histologically or cytologically confirmed diagnosis of advanced serous or endometrioid ovarian (regardless of the grade), primary...
- Must have progression on prior therapy documented radiographically and must have at least 1 measurable lesion (not previously irradiated) that can be...
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Adequate organ and bone marrow function, as described in the protocol
- Platinum-Resistant Ovarian Cancer, as described in the protocol Key
You likely can't join if
- Major surgical procedure or significant traumatic injury within 4 weeks prior to first dose of study intervention(s)
- Documented allergic or acute hypersensitivity reaction attributed to antibody treatments or doxorubicin hydrochloride or components of study...
- Another malignancy that is progressing or requires active treatment, as described in the protocol
- Untreated or active Central Nervous System (CNS) metastases, or carcinomatous meningitis, as described in the protocol
- Uncontrolled infections including but not limited to human immunodeficiency virus, hepatitis B or hepatitis C infection, or diagnosis of...
- Moderate to large or ascites, as described in the protocol
See the full eligibility criteria
- Participants with histologically or cytologically confirmed diagnosis of advanced serous or endometrioid ovarian (regardless of the grade), primary peritoneal, or fallopian tube cancer (clear cell, mucinous, and...
- Must have progression on prior therapy documented radiographically and must have at least 1 measurable lesion (not previously irradiated) that can be accurately measured by RECIST 1.1
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Adequate organ and bone marrow function, as described in the protocol
- Platinum-Resistant Ovarian Cancer, as described in the protocol Key
- Major surgical procedure or significant traumatic injury within 4 weeks prior to first dose of study intervention(s)
- Documented allergic or acute hypersensitivity reaction attributed to antibody treatments or doxorubicin hydrochloride or components of study intervention(s)
- Another malignancy that is progressing or requires active treatment, as described in the protocol
- Untreated or active Central Nervous System (CNS) metastases, or carcinomatous meningitis, as described in the protocol
- Uncontrolled infections including but not limited to human immunodeficiency virus, hepatitis B or hepatitis C infection, or diagnosis of immunodeficiency
- Moderate to large or ascites, as described in the protocol
- Bowel obstruction within last 3 months or current need for parenteral nutrition NOTE: Other protocol-defined inclusion/exclusion criteria apply
The study team makes the final eligibility decision.
Where it is enrolling
- Birmingham, Alabama, United States
- La Jolla, California, United States
- Los Angeles, California, United States
- Jacksonville, Florida, United States
- Miami, Florida, United States
- Orlando, Florida, United States
- Tampa, Florida, United States
- Chicago, Illinois, United States
- Westwood, Kansas, United States
- Louisville, Kentucky, United States
- Boston, Massachusetts, United States
- Detroit, Michigan, United States
- Hilliard, Ohio, United States
- Portland, Oregon, United States
- Pittsburgh, Pennsylvania, United States
- Sioux Falls, South Dakota, United States
- Dallas, Texas, United States
- Seattle, Washington, United States
- Madison, Wisconsin, United States
- Milwaukee, Wisconsin, United States
+ 23 more site(s).
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 female, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
This study is enrolling now at Birmingham, Alabama, United States; La Jolla, California, United States; Los Angeles, California, United States; Jacksonville, Florida, United States; Miami, Florida, United States; Orlando, Florida, United States and 37 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.