- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07524855
A Study of JNJ-101684362 (HLD-0117) in Patients With Metastatic Breast Cancer (HLD-0117)
A Phase 1 Study of JNJ-101684362 (HLD-0117) in Patients With Estrogen Receptor Positive (ER+) Metastatic Breast Cancer (MBC)
The purpose of this study is to find out the maximum tolerated dose (MTD) and/or recommended dose(s) for expansion (RDEs) of JNJ-101684362 (HLD-0117), to evaluate the safety of JNJ-101684362 (HLD-0117) , and how well the participants can tolerate it in Part 1 (dose escalation) of the study.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Antatt)
Fase
- Fase 1
Kontakter og plasseringer
Studiekontakt
- Navn: Study Contact
- Telefonnummer: 844-434-4210
- E-post: Participate-In-This-Study1@its.jnj.com
Studiesteder
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Adelaide, Australia, 5000
- Rekruttering
- Cancer Research SA
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Connecticut
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New Haven, Connecticut, Forente stater, 06510
- Rekruttering
- Yale University School Of Medicine
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Florida
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Sarasota, Florida, Forente stater, 34236
- Rekruttering
- Florida Cancer Specialists
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Massachusetts
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Boston, Massachusetts, Forente stater, 02114
- Rekruttering
- Massachusetts General Hospital
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Tennessee
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Nashville, Tennessee, Forente stater, 37203
- Rekruttering
- SCRI Oncology Partners
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Texas
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San Antonio, Texas, Forente stater, 78229
- Rekruttering
- South Texas Accelerated Research Therapeutics, LLC (START)
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Virginia
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Fairfax, Virginia, Forente stater, 22031
- Rekruttering
- Next Virginia
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
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Female (assigned at birth), greater than or equal to (>=) 18 years old, and able to provide informed consent
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Histologically confirmed metastatic or locally advanced breast cancer
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Postmenopausal status defined by surgical or natural menopause, or ovarian suppression with a GnRH agonist
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Prior therapy including
- Must have received at least one endocrine therapy in the metastatic setting.
- Must have received at least one cyclin-dependent kinase (CDK) 4/6i, either in the adjuvant and/or metastatic setting.
- For Part 1 and Part 2 Cohorts 2A, 2B, 2C, and 2D: Participants may have received up to two prior distinct cytotoxic regimens (for example, taxanes, antibody-drug conjugates (ADCs), etc.) in the metastatic setting, unless discussed and approved by the medical monitor.
- For Part 2 Cohort 2E: Participants must have received more than two prior distinct cytotoxic regimens (for example, taxanes, ADCs, etc.) in the metastatic setting.
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Radiologic disease progression on the most recent therapy
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Patients must have disease evaluable per response evaluation criteria in solid tumors (RECIST) v1.1
- For Part 1 and Part 2B, 2C, and 2E: Participants may have either evaluable or measurable disease per RECIST v1.1.
- For Part 2 Cohort 2A: Participants should have measurable soft tissue disease per RECIST v1.1.
- For Part 2 Cohort 2D: Participants should have evaluable but not measurable disease.
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Willingness to provide baseline and on-treatment tumor biopsies, unless not feasible or medically appropriate
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For Part 1 and Part 2 (all cohorts):
- Participants must have documented >=10% ER staining and human epidermal growth factor receptor 2 (HER2) negative (per american society of clinical oncology [ASCO] college of american pathologists [CAP] guidelines) on the most recent tumor biopsy sample obtained.
- For Part 2 Cohort 2B: Participants must have recent estrogen receptor 1 gene (ESR1) wild type from tumor or circulating tumor deoxy ribonucleic acid (ctDNA) testing performed after the most recent endocrine therapy prior to enrollment.
- For Part 2 Cohort 2C: Participants must have ESR1 mutation detected from tumor or ctDNA testing performed prior to enrollment.
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Eastern cooperative oncology group (ECOG) performance status 0-1 and life expectancy of at least 3 months
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Adequate organ function Recovery from prior therapy-related toxicities to Grade <=1 (except alopecia; neuropathy and endocrinopathies <=Grade 2)
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Ability to swallow oral medication and comply with study procedures
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Stable dose (>=30 days) of bisphosphonates or denosumab, if applicable
Exclusion Criteria:
- Participants with Inflammatory breast cancer or leptomeningeal disease or brain metastases, with the exception of patients with definitively treated brain metastases that are clinically stable and asymptomatic for >2 weeks and who are off or receiving low-dose corticosteroid treatment (<=10 mg prednisone or equivalent) for at least 2 weeks prior to start of study treatment.
- Recent major bleeding or uncontrolled bleeding disorder
- Ongoing corticosteroid use >10 mg/day (prednisone equivalent)
- Recent anticancer or investigational therapy within 14 days (28 days for fulvestrant)
- Untreated or unstable spinal cord compression
- Significant cardiovascular disease within 6 months or ongoing uncontrolled cardiac conditions
- Active or uncontrolled infection (controlled HIV or treated hepatitis C allowed)
- Uncontrolled renal, pancreatic, or liver disease (excluding stable conditions such as Gilbert's syndrome or liver metastases)
- Another malignancy requiring treatment within 2 years (except low-risk, curatively treated cancers)
- Major surgery within 28 days
- Any condition that may interfere with safety or study compliance
- Pregnancy or breastfeeding
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Sekvensiell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: Arm 1
JNJ-101684362 (HLD-0117): Participants with estrogen receptor positive (ER+) metastatic breast cancer (MBC) will receive JNJ-101684362 (HLD-0117) orally once daily as monotherapy in Part 1 until recommended dose(s) for expansion has been developed. Participants in Part 2 will receive JNJ-101684362 (HLD-0117) at the RP2Ds developed in Part 1. |
A treatment cycle consists of 28 days. Treatment may continue until disease progression or study discontinuation (withdrawal of consent, intercurrent illness, unacceptable adverse event or any other changes unacceptable for further treatment, etc.) |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Dose Limiting Toxicities (DLTs)
Tidsramme: 28 days
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Frequency of dose-limiting toxicities (DLTs) |
28 days
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AEs, ECGs, Labs and Clinical Changes
Tidsramme: 28 days
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Frequency and severity of adverse events (AEs) and abnormal electrocardiogram (ECG), laboratory and clinical changes from baseline |
28 days
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Objective response rate (ORR)
Tidsramme: 56 Days
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Objective response rate (ORR) per RECIST in evaluable patients |
56 Days
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Duration of response (DOR)
Tidsramme: 28 days
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DOR is defined as the time from the first occurrence of a documented objective response to disease progression or death from any cause, whichever occurs first. |
28 days
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Progression-free survival (rPFS)
Tidsramme: 56 days
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Radiographic progression-free survival (rPFS) |
56 days
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Disease Control Rate (DCR)
Tidsramme: 24 weeks
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Disease Control Rate (DCR) |
24 weeks
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Clinical Benefit Rate (CBR)
Tidsramme: 24 weeks
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CBR is defined as the proportion of patients who achieve partial response (PR) or complete response (CR), or stable disease (SD) lasting at least 24 weeks, as assessed according to RECIST v1.1. |
24 weeks
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Samarbeidspartnere og etterforskere
Etterforskere
- Studieleder: Janssen Research & Development, LLC Clinical Trial, Janssen Research & Development, LLC
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- HLD-0117-ONC-101
- HLD-0117-ONC-101 (Annen identifikator: Janssen Research & Development, LLC)
- 2026-527749-23-00 (Registeridentifikator: EUCT number)
Plan for individuelle deltakerdata (IPD)
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