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A Study Evaluating The PF-03084014 In Combination With Docetaxel In Patients With Advanced Breast Cancer

Pfizer logo

Pfizer

Status and phase

Terminated
Phase 1

Conditions

Breast Cancer Metastatic

Treatments

Drug: PF-03084014
Drug: Docetaxel

Study type

Interventional

Funder types

Industry

Identifiers

NCT01876251
2013-000659-41 (EudraCT Number)
A8641016

Details and patient eligibility

About

This study is aimed to determine the tolerability of the PF-03084014 plus docetaxel combination in patients with advanced breast cancer. Preliminary information about the efficacy of the combination will also be collected.

Enrollment

30 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of breast cancer with evidence of a) metastatic or b) locally recurrent/advanced disease.

Exclusion criteria

  • Prior treatment with a gamma secretase inhibitors or other Notch signaling inhibitors.

Trial design

30 participants in 1 patient group

PF-03084014 plus docetaxel
Experimental group
Description:
PF 03084014 will be administered orally, continuously, twice daily at doses from 80 to 150 mg in combination with docetaxel given every 3 weeks at doses from 75 to 100 mg/m\^2
Treatment:
Drug: PF-03084014
Drug: PF-03084014
Drug: Docetaxel
Drug: Docetaxel
Drug: PF-03084014

Trial contacts and locations

16

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Data sourced from clinicaltrials.gov

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