TACTIVE-U: Tutkimus, jolla opit opiskelulääkkeestä (Vepdegestrant), kun sitä annetaan muiden lääkkeiden kanssa ihmisille, joilla on pitkälle edennyt tai metastaattinen rintasyöpä. (alatutkimus C)
TACTIVE-U: TURVALLISUUDEN JA TEHOKKUUDEN TUTKIMUS VAIHE 1B/2, AVOIN KÄYTETTÄVÄ TUTKIMUS VEPDEGESTRANTIN SIEDETTÄVYYDEN, PK:n ja kasvainten vastaisen toiminnan tutkimiseksi (ARV-471/PF-SISIFORTAALTEANY0322-07885). YHDISTELMÄ MUUN KANSSA Syövän vastaiset hoidot 18-Vuotiaille ja sitä vanhemmille OSALLISTUJILLE, JOLLA ON EDETTYNYT TAI METASTAATTISIA RINTASyöpää, ALATUTKIMUS C (ARV-471 YHDESSÄ SAMURACICLIBIN KANSSA)
The purpose of this study is to learn about the safety and effects of the study medicine called vepdegestrant. The safety and effects of vepdegestrant will be see when given with other medicines. Vepdegestrant is studied to see if it can be a possible treatment for advanced metastatic breast cancer. This type of cancer would have spread from where it started (breast) to other parts of the body and would be tough to treat.
The study is seeking for participants who have breast cancer that:
- is hard to treat (advanced) and may have spread to other organs (metastatic). is sensitive to hormonal therapy (it is called estrogen receptor positive).
- is no longer responding to treatments taken before starting this study.
This study is divided into separate sub-studies.
For Sub-Study C:
All the participants will receive vepdegestrant and a medicine called samuraciclib.
Vepdegestrant and samuraciclib will be taken once in a day by mouth. The medicines will be taken at home. The experience of people receiving the study medicines will be studied. This will help see if the study medicine is safe and effective.
Participant will continue to take vepdegestrant and samuraciclib until:
- their cancer is no longer responding, or
- side effects become too severe.
They will have visits at the study clinic about every 4 weeks.
Tutkimuksen yleiskatsaus
Yksityiskohtainen kuvaus
C4891024 is a prospective, open-label, multicenter, Phase 1b/2 sub-study to evaluate the safety, antitumor activity, and PK of ARV-471 with samuraciclib in the treatment of participants with A/MBC. The sub-study is part of Umbrella platform, TACTIVE-U, comprising multiple sub-studies that independently evaluate ARV-471 in participants with Estrogen Receptor Positive/Human Epidermal Growth Factor Receptor 2 Negative (ER+/HER2-) Advanced or Metastatic Breast Cancer. ARV-471 will act as the backbone therapy given in combination with other anticancer agents thought to have clinical relevance in ER+ breast cancer.
Opintotyyppi
Ilmoittautuminen (Todellinen)
Vaihe
- Vaihe 2
- Vaihe 1
Yhteystiedot ja paikat
Opiskelupaikat
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Bruxelles-capitale, Région de
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Anderlecht, Bruxelles-capitale, Région de, Belgia, 1070
- Institut Jules Bordet
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-
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Roma, Italia, 00168
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS - Università Cattolica del Sacro Cuore
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Lombardy
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Monza, Lombardy, Italia, 20900
- Fondazione IRCCS San Gerardo dei Tintori
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Côte-d'or
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Dijon, Côte-d'or, Ranska, 21079
- Centre Georges François Leclerc
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Arkansas
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Fayetteville, Arkansas, Yhdysvallat, 72703
- Highlands Oncology Group
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Rogers, Arkansas, Yhdysvallat, 72758
- Highlands Oncology Group
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Springdale, Arkansas, Yhdysvallat, 72762
- Highlands Oncology Group
-
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California
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Palo Alto, California, Yhdysvallat, 94304
- Stanford Women's Cancer Center
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Palo Alto, California, Yhdysvallat, 94304
- Clinical and Translational Research Unit (CTRU)
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Palo Alto, California, Yhdysvallat, 94304
- Stanford Cancer Institute - Clinical Trials Office
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Colorado
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Fort Collins, Colorado, Yhdysvallat, 80524
- UCHealth Poudre Valley Hospital
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Fort Collins, Colorado, Yhdysvallat, 80528
- UCHealth Harmony
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Greeley, Colorado, Yhdysvallat, 80634
- UCHealth Greeley Hospital
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Loveland, Colorado, Yhdysvallat, 80538
- UCHealth - Medical Center of the Rockies
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Illinois
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Shiloh, Illinois, Yhdysvallat, 62269
- Memorial Hospital East
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Shiloh, Illinois, Yhdysvallat, 62269
- Siteman Cancer Center - Shiloh
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Missouri
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City of Saint Peters, Missouri, Yhdysvallat, 63376
- Siteman Cancer Center - St Peters
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Creve Coeur, Missouri, Yhdysvallat, 63141
- Siteman Cancer Center - West County
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Florissant, Missouri, Yhdysvallat, 63031
- Siteman Cancer Center - North County
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St Louis, Missouri, Yhdysvallat, 63110
- Barnes-Jewish Hospital
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St Louis, Missouri, Yhdysvallat, 63110
- Washington University School of Medicine
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St Louis, Missouri, Yhdysvallat, 63110
- Washington University School of Medicine - Siteman Cancer Center
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St Louis, Missouri, Yhdysvallat, 63129
- Siteman Cancer Center - South County
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Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
Inclusion Criteria:
- Histological or cytological diagnosis of breast cancer. At time of enrollment this must not be amendable to surgical resection with curative intent (≥1% ER+ stained cells as per local practice on the most recent tumor biopsy HER2- tumor by IHC or in-situ hybridization per ASCO/CAP).
- prior anticancer therapies: up to 2 lines of prior therapies for advanced/metastatic disease; 1 line of any CDK4/6 inhibitor-based regimen is required (in any setting eg adjuvant, metastatic)
- at least 1 measurable lesion as defined by RECIST v1.1.
- ECOG PS ≤1.
Exclusion Criteria:
- visceral crisis at risk of life-threatening complications in the short term
- known history of drug-induced pneumonitis or other significant symptomatic deterioration of lung functions.
- newly diagnosed brain metastases, or symptomatic CNS metastases, carcinomatous meningitis, or leptomeningeal disease. Participants with a history of CNS metastases or cord compression are eligible if they have been definitively treated, clinically stable and discontinued anti-seizure medications and corticosteroids for at least 28 days prior to enrollment in the of study.
- history of any other tumor malignancies within the past 3 years, except for the following: (1) adequately treated basal or squamous cell carcinoma of the skin; (2) curatively treated in situ carcinoma of the cervix.
- inflammatory breast cancer
- impaired cardiovascular function or clinically significant cardiovascular diseases
- concurrent administration of medications, food, or herb supplements that are strong inhibitors/inducers of CYP3A, strong CYP2D6 inhibitors and drugs known to predispose to Torsade de Pointes or QT interval prolongation.
- renal impairment, not adequate liver function and/or bone marrow function
- known active infection
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Ei käytössä
- Inventiomalli: Peräkkäinen tehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
|
Kokeellinen: ARV-471 in combination with Samuraciclib
ARV-471 administered orally QD continuously and Samuraciclib administered orally QD continuously on 28-day cycles |
Daily oral dosages of ARV-471 continuously, dose escalation/de-escalation in Phase 1b until RP2D determined, cycles lasting 28 days
Muut nimet:
Daily oral dosages of Samuraciclib continuously, dose escalation/de-escalation in Phase 1b until RP2D determined, cycles lasting 28 days |
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Phase 1b: Number of Participants With Dose Limiting Toxicities
Aikaikkuna: 28 days
|
Dose Limiting Toxicities rate for ARV-471 in combination with Samuraciclib, estimated based on data from DLT-evaluable participants during the DLT observation period (Cycle 1). |
28 days
|
|
Drug Drug Interaction: To evaluate the effect of samuraciclib on PK of ARV 471.
Aikaikkuna: From the start of Lead-in period (maximum 13 days) to the end of cycle 1 (at least 28 days)
|
Steady-state Area under the plasma concentration versus time curve (AUCtau) of ARV-471 with and without coadministration of samuraciclib |
From the start of Lead-in period (maximum 13 days) to the end of cycle 1 (at least 28 days)
|
|
Drug Drug Interaction: To evaluate the effect of samuraciclib on PK of ARV 471.
Aikaikkuna: From the start of Lead-in period (maximum 13 days) to the end of cycle 1 (at least 28 days)
|
Steady-state Peak Plasma concentration ( Cmax) of ARV-471 with and without coadministration of samuraciclib |
From the start of Lead-in period (maximum 13 days) to the end of cycle 1 (at least 28 days)
|
|
Phase 2: Percentage of Participants With Objective Response by investigator assessment
Aikaikkuna: Up to approximately 1 year
|
Objective response (OR) refers to confirmed complete response (CR) or partial response (PR) according to Response Evaluation Criteria in Solid Tumor (RECIST) version 1.1. as determined by investigator assessment. |
Up to approximately 1 year
|
|
Drug Drug Interaction: • To evaluate the effect of ARV 471 on PK of samuraciclib.
Aikaikkuna: From the start of Lead-in period (maximum 13 days) to the end of cycle 1 (at least 28 days))
|
Single dose AUC0-72 of samuraciclib with and without coadministration of ARV 471. |
From the start of Lead-in period (maximum 13 days) to the end of cycle 1 (at least 28 days))
|
|
Drug Drug Interaction: • To evaluate the effect of ARV 471 on PK of samuraciclib.
Aikaikkuna: From the start of Lead-in period (maximum 13 days) to the end of cycle 1 (at least 28 days))
|
Single dose Cmax of samuraciclib with and without coadministration of ARV 471. |
From the start of Lead-in period (maximum 13 days) to the end of cycle 1 (at least 28 days))
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Phase 1b, Drug drug interaction and Phase 2: Evaluation of Safety and Tolerability of ARV-471 in combination with Samuraciclib
Aikaikkuna: First study drug dose through a minimum of 28 Days After Last study drug administration
|
AEs as characterized by type, frequency, intensity as graded by NCI CTCAE version 5.0, timing, seriousness, and relationship to ARV-471 in combination with samuraciclib. Laboratory test abnormalities as characterized by type, frequency, intensity (as graded by NCI CTCAE version 5.0), and timing. Changes from baseline for the ECG parameters heart rate, QTcF, PR interval, and QRS complex will be summarized by treatment and time. The frequency of uncorrected QT values above 500 ms will be tabulated. |
First study drug dose through a minimum of 28 Days After Last study drug administration
|
|
Phase 1b: To evaluate antitumor activity of ARV-471 in combination with samuraciclib
Aikaikkuna: Up to approximately 1 year
|
Objective response (OR) refers to confirmed complete response (CR) or partial response (PR) according to Response Evaluation Criteria in Solid Tumor (RECIST) version 1.1. as determined by investigator assessment. |
Up to approximately 1 year
|
|
Phase 1b and Phase 2: Duration of Response by investigator assessment.
Aikaikkuna: Up to approximately 1 year
|
Duration of Response (DoR) is defined for participants with confirmed OR (CR or PR) as the time from the first documentation of OR to the first documentation of objective tumor progression or to death due to any cause, whichever occurs first. |
Up to approximately 1 year
|
|
Phase 1b and Phase2: Percentage of participants with Clinical Benefit Response by investigator assessment.
Aikaikkuna: Up to approximately 1 year
|
Clinical Benefit Response (CBR) is defined as the proportion of participants with Best Overall Response of confirmed CR or PR at any time, or Stable Disease (SD) ≥24 weeks |
Up to approximately 1 year
|
|
Phase 1b and Phase 2: Progression Free Survival by investigator assessment.
Aikaikkuna: Up to approximately 1 year
|
Progression Free Survival (PFS) is defined as the time from the date of first dose of study interventions to the date of first documentation of PD or death due to any cause, whichever occurs first. |
Up to approximately 1 year
|
|
Phase 1b and Phase 2: Plasma concentrations of ARV-471 and samuraciclib.
Aikaikkuna: At predefined intervals throughout the treatment period, up to cycle 7 (each cycle is 28 days)
|
To evaluate the plasma exposure of ARV-471 and samuraciclib when ARV-471 and samuraciclib are given in combination. |
At predefined intervals throughout the treatment period, up to cycle 7 (each cycle is 28 days)
|
|
Phase 1b: Evaluation of effect of samuraciclib on PK of ARV-471
Aikaikkuna: At predefined intervals throughout the treatment period, up to cycle 7 (each cycle is 28 days)
|
AUCtau of ARV-471 with and without co-administration of samuraciclib |
At predefined intervals throughout the treatment period, up to cycle 7 (each cycle is 28 days)
|
|
Phase 1b: Evaluation of effect of samuraciclib on PK of ARV-471
Aikaikkuna: At predefined intervals throughout the treatment period, up to cycle 7 (each cycle is 28 days)
|
Cmax of ARV-471 with and without co-administration of samuraciclib |
At predefined intervals throughout the treatment period, up to cycle 7 (each cycle is 28 days)
|
|
Phase 2:ctDNA plasma quantitative changes from pre-treatment
Aikaikkuna: At predefined intervals throughout the treatment period, up to cycle 3 (each cycle is 28 days) and end of treatment
|
To assess changes from baseline levels in plasma ctDNA with treatment and to evaluate potential predictability of their associations with clinical outcomes. |
At predefined intervals throughout the treatment period, up to cycle 3 (each cycle is 28 days) and end of treatment
|
|
Phase 2: To evaluate the correlation between TP53 mutation status and antitumor activity
Aikaikkuna: Screening
|
Participants classified on basis of pathological TP53 mutation detected or not detected. |
Screening
|
|
Phase 2: Overall Survival
Aikaikkuna: Through study completion, up to approximately 3 year
|
Overall Survival (OS) is defined as the time from the date of first dose of study interventions to the date of death due to any cause |
Through study completion, up to approximately 3 year
|
Yhteistyökumppanit ja tutkijat
Sponsori
Yhteistyökumppanit
Tutkijat
- Opintojohtaja: Pfizer CT.gov Call Center, Pfizer
Julkaisuja ja hyödyllisiä linkkejä
Hyödyllisiä linkkejä
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Todellinen)
Ensisijainen valmistuminen (Todellinen)
Opintojen valmistuminen (Todellinen)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Muita asiaankuuluvia MeSH-ehtoja
Muut tutkimustunnusnumerot
- C4891024
- 2023-507125-41-00 (Rekisterin tunniste: CTIS (EU))
- 2023 (Yhdysvaltain NIH-apuraha/sopimus)
Yksittäisten osallistujien tietojen suunnitelma (IPD)
Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?
IPD-suunnitelman kuvaus
Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests.
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