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NCT04606446RECRUITINGanonymous

A PHASE 1/2A DOSE ESCALATION AND EXPANSION STUDY TO EVALUATE SAFETY, TOLERABILITY, PHARMACOKINETIC, PHARMACODYNAMIC, AND ANTI-TUMOR ACTIVITY OF PF-07248144 IN PARTICIPANTS WITH ADVANCED OR METASTATIC SOLID TUMORS

Sponsor

Source record

Pfizer

Phase

Source record

Phase 1/2A

Modality

AI-normalized

small molecule

Target

AI-normalized

KAT6 Inhibitor

Indication / condition

AI-normalized

Locally Advanced or Metastatic ER+ HER2- Breast Cancer

Intervention

Source record

PF-07248144, Fulvestrant, Letrozole, Palbociclib, PF-07220060, PF-07850327, ARV-471, vepdegestrant

Source & freshness

Source record

NCT ID

NCT04606446

Original source

ClinicalTrials.gov

Source last updated

Apr 16, 2026

Ingested at

Jun 12, 2026

Internal sync

Jun 12, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT04606446

Title

A PHASE 1/2A DOSE ESCALATION AND EXPANSION STUDY TO EVALUATE SAFETY, TOLERABILITY, PHARMACOKINETIC, PHARMACODYNAMIC, AND ANTI-TUMOR ACTIVITY OF PF-07248144 IN PARTICIPANTS WITH ADVANCED OR METASTATIC SOLID TUMORS

Sponsor

Pfizer

Status

RECRUITING

Phase

Phase 1/2A

Condition raw

Locally Advanced or Metastatic ER+ HER2- Breast Cancer, Locally Advanced or Metastatic Castration-resistant Prostate Cancer, Locally Advanced or Metastatic Non-small Cell Lung Cancer

Condition normalized

Locally Advanced or Metastatic ER+ HER2- Breast Cancer, Locally Advanced or Metastatic Castration-resistant Prostate Cancer, Locally Advanced or Metastatic Non-small Cell Lung Cancer

Modality raw

small molecule

Modality normalized

small molecule

Target raw

KAT6 Inhibitor

Target normalized

KAT6 Inhibitor

Interventions

PF-07248144, Fulvestrant, Letrozole, Palbociclib, PF-07220060, PF-07850327, ARV-471, vepdegestrant

Public preview

Source record

PF-07248144, developed by Pfizer, is currently undergoing a Phase 1/2A clinical trial targeting advanced or metastatic solid tumors, specifically focusing on ER+HER2- breast cancer, castration-resistant prostate cancer (CRPC), and non-small cell lung cancer (NSCLC). The trial's design includes both monotherapy and combination therapy approaches, which may enhance its market potential by addressing treatment-resistant cancers. The competitive landscape includes established therapies such as CDK4/6 inhibitors and endocrine therapies, necessitating a strong efficacy and safety profile to differentiate PF-07248144. Given the increasing prevalence of these cancers and the demand for novel treatment options, successful outcomes could position PF-07248144 favorably within a lucrative oncology market. The estimated enrollment of 320 participants indicates a robust commitment to generating significant clinical data, which could attract interest from investors and stakeholders in the oncology space.

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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