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NCT06206837ACTIVE_NOT_RECRUITINGanonymous

AN INTERVENTIONAL SAFETY AND EFFICACY PHASE 1B/2, OPEN-LABEL STUDY TO INVESTIGATE TOLERABILITY, PK, AND ANTITUMOR ACTIVITY OF VEPDEGESTRANT (ARV-471/PF-07850327), AN ORAL PROTEOLYSIS TARGETING CHIMERA, IN COMBINATION WITH PF-07220060 IN PARTICIPANTS AGED 18 YEARS AND OLDER WITH ER+/HER2- ADVANCED OR METASTATIC BREAST CANCER

Sponsor

Source record

Pfizer

Phase

Source record

Phase 1B/2

Modality

AI-normalized

small molecule

Target

AI-normalized

Oral proteolysis targeting chimera (PROTAC) mechanism targeting estrogen receptors in ER+/HER2- advanced or metastatic breast cancer.

Indication / condition

AI-normalized

Breast Cancer

Intervention

Source record

vepdegestrant, PF-07220060

Source & freshness

Source record

NCT ID

NCT06206837

Original source

ClinicalTrials.gov

Source last updated

Feb 27, 2026

Ingested at

Jun 13, 2026

Internal sync

Jun 13, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT06206837

Title

AN INTERVENTIONAL SAFETY AND EFFICACY PHASE 1B/2, OPEN-LABEL STUDY TO INVESTIGATE TOLERABILITY, PK, AND ANTITUMOR ACTIVITY OF VEPDEGESTRANT (ARV-471/PF-07850327), AN ORAL PROTEOLYSIS TARGETING CHIMERA, IN COMBINATION WITH PF-07220060 IN PARTICIPANTS AGED 18 YEARS AND OLDER WITH ER+/HER2- ADVANCED OR METASTATIC BREAST CANCER

Sponsor

Pfizer

Status

ACTIVE_NOT_RECRUITING

Phase

Phase 1B/2

Condition raw

Breast Cancer

Condition normalized

Breast Cancer

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Oral proteolysis targeting chimera (PROTAC) mechanism targeting estrogen receptors in ER+/HER2- advanced or metastatic breast cancer.

Target normalized

Oral proteolysis targeting chimera (PROTAC) mechanism targeting estrogen receptors in ER+/HER2- advanced or metastatic breast cancer.

Interventions

vepdegestrant, PF-07220060

Public preview

Source record

The clinical trial for vepdegestrant (ARV-471/PF-07850327) in combination with PF-07220060 represents a strategic initiative by Pfizer to address the unmet medical need in advanced or metastatic ER+/HER2- breast cancer, a significant segment of the oncology market. The trial's design, which includes a sequential approach to dose escalation and evaluation of safety and efficacy, positions Pfizer to potentially capture market share in a competitive landscape dominated by existing therapies such as CDK4/6 inhibitors and hormonal therapies. The combination therapy may offer a novel mechanism of action, enhancing treatment options for patients who have exhausted standard therapies. The trial's outcomes could influence future treatment guidelines and establish a new standard of care, thereby impacting Pfizer's market positioning and revenue potential in oncology.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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