New pill shows promise for Hard-to-Treat breast cancer
NCT ID NCT04115306
First seen Jun 27, 2026 · Last updated Jul 17, 2026 · Updated 2 times
Summary
This study tests an experimental oral drug called PMD-026 in people with metastatic breast cancer that has spread and is no longer curable. The drug targets a protein called RSK2 found in some tumors. The trial will check safety and how well the drug works alone or with another hormone therapy (fulvestrant). About 61 participants will be enrolled.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- PMD-026 (oral targeted drug) and fulvestrant (hormone therapy)
- What this could lead to
- If successful, this could lead to a new oral treatment option for people with a specific type of advanced breast cancer that has stopped responding to other therapies.
- What could go wrong
- This is an early-phase trial with only 61 participants, so the drug may not prove effective or safe enough for wider use. Side effects are unknown at this stage.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
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About 61 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2019
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria, Combination with fulvestrant (Part 3): * RSK2 positive from available archival or fresh tumor tissue (FFPE). * Histologically or cytologically diagnosed HR+, HER2- * ESR1 wild type * Diagnosis of adenocarcinoma of the breast with evidence of either locally advanced disease not amendable to resection or radiation with curative intent or metastatic disease not amendable to curative therapy * Must be appropriate candidates for endocrine therapy * Previously received at least 1 line of endocrine therapy for MBC or had recurrence while on adjuvant endocrine therapy for locally advanced breast cancer * Discontinued endocrine therapy at least 15 days prior to first dose of PMD-026 * At least 1 measurable target lesion as defined by RECIST v1.1 * Progression on or after treatment with a CDK4/6 inhibitor in combination with endocrine therapy inhibitor in the locally advanced or metastatic setting * Adequate hematologic, hepatic, and renal function as assessed by laboratory parameters * Toxicity related to prior therapy resolved to at least Grade 1 (alopecia excepted) or to at least Grade 2 with prior approval of the Medical Monitor Exclusion Criteria, Combination with fulvestrant (Part 3): * Prior chemotherapy * ESR1 mutations * ≤14 days from biological or investigational therapy * Presence of visceral crisis or uncontrolled visceral disease for which chemotherapy would be indicated * Central nervous system metastases, unless appropriately treated and neurologically stable * History of leptomeningeal metastases * Active, uncontrolled bacterial, viral, or fungal infection(s) requiring systemic therapy * Known hepatitis B or hepatitis C infection * Known HIV-positive with CD4+ cell counts \<350 cells/μL * Known HIV-positive with a history of an AIDS-defining opportunistic infection * History of clinically significant cardiovascular abnormalities, including QTcF interval \>460 msec (using Fridericia's formula)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Banner MD Anderson Cancer Center
Gilbert, Arizona, 85234, United States
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City of Hope
Duarte, California, 91010, United States
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City of Hope Chicago
Zion, Illinois, 60099, United States
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City of Hope Orange County, Lennar
Irvine, California, 92618, United States
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Massachusetts General Hospital Cancer Center
Boston, Massachusetts, 02114, United States
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Moffitt Cancer Center
Tampa, Florida, 33612, United States
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Ohio State University
Columbus, Ohio, 43210, United States
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Profound Research
Farmington Hills, Michigan, 48334, United States
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South Texas Accelerated Research Therapeutics
San Antonio, Texas, 78229, United States
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University of California, Los Angeles (UCLA)
Los Angeles, California, 90095, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can an oral drug replace injections for advanced breast cancer?
- Can a Three-Drug combo crack Triple-Negative breast cancer?
- Can a blood test reveal when breast cancer treatment stops working?
- New antibody aims to preserve immune checkpoint while fighting cancer
- Zapping a few growing tumors may keep breast cancer drugs working longer
- Can a Two-Drug combo outsmart resistant breast and ovarian cancers?