TACTIVE-U: A Study to Learn About the Study Medicine (Vepdegestrant) When Given With Other Medicines in People With Advanced or Metastatic Breast Cancer. (Sub-Study C)

Breast Cancer Clinical Trial

Official title:

TACTIVE-U: AN INTERVENTIONAL SAFETY AND EFFICACY PHASE 1B/2, OPEN-LABEL UMBRELLA STUDY TO INVESTIGATE TOLERABILITY, PK, AND ANTITUMOR ACTIVITY OF VEPDEGESTRANT (ARV-471/PF-07850327), AN ORAL PROTEOLYSIS TARGETING CHIMERA, IN COMBINATION WITH OTHER ANTICANCER TREATMENTS IN PARTICIPANTS AGED 18 AND OLDER WITH ER+ ADVANCED OR METASTATIC BREAST CANCER, SUB-STUDY C (ARV-471 IN COMBINATION WITH SAMURACICLIB)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06125522
• Other study ID #: C4891024
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: January 10, 2024
• Est. completion date: January 25, 2027

Study information

• Verified date: April 2024
• Source: Pfizer
• Contact: Pfizer CT.gov Call Center
• Phone: 1-800-718-1021
• Email: ClinicalTrials.gov_Inquiries[@]pfizer.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 67
• Est. completion date: January 25, 2027
• Est. primary completion date: July 23, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• vepdegestrant
Daily oral dosages of ARV-471 continuously, dose escalation/de-escalation in Phase 1b until RP2D determined, cycles lasting 28 days
• Samuraciclib
Daily oral dosages of Samuraciclib continuously, dose escalation/de-escalation in Phase 1b until RP2D determined, cycles lasting 28 days

Locations

Country	Name	City	State
Belgium	Institut Jules Bordet	Anderlecht	Bruxelles-capitale, Région DE
Belgium	Antwerp University Hospital	Edegem	Antwerpen
Puerto Rico	BRCR Global - Mayagüez	Mayaguez
Puerto Rico	Pan American Center for Oncology Trials, LLC	Rio Piedras
United States	Siteman Cancer Center - West County	Creve Coeur	Missouri
United States	Highlands Oncology Group	Fayetteville	Arkansas
United States	Siteman Cancer Center - North County	Florissant	Missouri
United States	UCHealth Harmony	Fort Collins	Colorado
United States	UCHealth Poudre Valley Hospital	Fort Collins	Colorado
United States	UCHealth Greeley Hospital	Greeley	Colorado
United States	UCHealth - Medical Center of the Rockies	Loveland	Colorado
United States	Highlands Oncology Group	Rogers	Arkansas
United States	Barnes-Jewish Hospital	Saint Louis	Missouri
United States	Siteman Cancer Center - South County	Saint Louis	Missouri
United States	Washington University School of Medicine	Saint Louis	Missouri
United States	Washington University School of Medicine - Siteman Cancer Center	Saint Louis	Missouri
United States	Siteman Cancer Center - St Peters	Saint Peters	Missouri
United States	Memorial Hospital East	Shiloh	Illinois
United States	Siteman Cancer Center - Shiloh	Shiloh	Illinois
United States	Highlands Oncology Group	Springdale	Arkansas

Sponsors (3)

Lead Sponsor	Collaborator
Pfizer	Arvinas Estrogen Receptor, Inc., Carrick Therapeutics Limited

Countries where clinical trial is conducted

United States,  Belgium,  Puerto Rico, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Phase 1b: Number of Participants With Dose Limiting Toxicities	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
Primary	Drug Drug Interaction: To evaluate the effect of samuraciclib on PK of ARV 471.	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)
Primary	Drug Drug Interaction: To evaluate the effect of samuraciclib on PK of ARV 471.	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)
Primary	Phase 2: Percentage of Participants With Objective Response by investigator assessment	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
Primary	Drug Drug Interaction: • To evaluate the effect of ARV 471 on PK of samuraciclib.	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))
Primary	Drug Drug Interaction: • To evaluate the effect of ARV 471 on PK of samuraciclib.	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))
Secondary	Phase 1b, Drug drug interaction and Phase 2: Evaluation of Safety and Tolerability of ARV-471 in combination with Samuraciclib	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
Secondary	Phase 1b: To evaluate antitumor activity of ARV-471 in combination with samuraciclib	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
Secondary	Phase 1b and Phase 2: Duration of Response by investigator assessment.	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
Secondary	Phase 1b and Phase2: Percentage of participants with Clinical Benefit Response by investigator assessment.	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
Secondary	Phase 1b and Phase 2: Progression Free Survival by investigator assessment.	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
Secondary	Phase 1b and Phase 2: Plasma concentrations of ARV-471 and samuraciclib.	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)
Secondary	Phase 1b: Evaluation of effect of samuraciclib on PK of ARV-471	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)
Secondary	Phase 1b: Evaluation of effect of samuraciclib on PK of ARV-471	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)
Secondary	Phase 2:ctDNA plasma quantitative changes from pre-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
Secondary	Phase 2: To evaluate the correlation between TP53 mutation status and antitumor activity	Participants classified on basis of pathological TP53 mutation detected or not detected.	Screening
Secondary	Phase 2: Overall Survival	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

External Links

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