Expanded Access Study Of Palbociclib (PD-0332991) In Combination With Letrozole As Treatment Of Post-Menopausal Women With HR-Positive, Her2-Negative Advanced Breast Cancer For Whom Letrozole Therapy Is Deemed Appropriate
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ClinicalTrials.gov Identifier: NCT02142868 |
Expanded Access Status :
No longer available
First Posted : May 20, 2014
Last Update Posted : December 21, 2018
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Condition or disease | Intervention/treatment |
---|---|
Advanced Breast Cancer (Female) | Drug: Palbociclib Drug: Letrozole |
Study Type : | Expanded Access |
Expanded Access Type : | Individual Patients |
Official Title: | AN EXPANDED ACCESS STUDY OF PALBOCICLIB IN COMBINATION WITH LETROZOLE AS TREATMENT OF POST-MENOPAUSAL WOMEN WITH HORMONE RECEPTOR POSITIVE, HER2 NEGATIVE ADVANCED BREAST CANCER FOR WHOM LETROZOLE THERAPY IS DEEMED APPROPRIATE |

- Drug: Palbociclib
Palbociclib will be administered orally once a day at 125 mg/day for 21 days followed by 7 days off treatment for each 28-day cycle (Schedule 3/1)Other Name: Ibrance
- Drug: Letrozole
Letrozole will be administered orally at 2.5 mg once daily as continuous daily dosing schedule according to product labeling and in compliance with its local prescribing information.Other Name: Femara

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | Female |
Gender Based Eligibility: | Yes |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Post-menopausal women 18 years of age or above with proven diagnosis of advanced adenocarcinoma of the breast (locoregionally recurrent or metastatic disease)
- ER-positive and/or PR-positive tumor based on local laboratory results
- HER2-negative tumor based on local laboratory results
- Patients must be appropriate candidates for letrozole therapy (Canada: first-line patients only)
Exclusion Criteria:
- Patients who have previously participated in a palbociclib trial or who have received prior treatment with any CDK inhibitor

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02142868

Study Director: | Pfizer CT.gov Call Center | Pfizer |
Responsible Party: | Pfizer |
ClinicalTrials.gov Identifier: | NCT02142868 |
Other Study ID Numbers: |
A5481034 |
First Posted: | May 20, 2014 Key Record Dates |
Last Update Posted: | December 21, 2018 |
Last Verified: | December 2018 |
Expanded Access Advanced Breast Cancer |
Breast Neoplasms Neoplasms by Site Neoplasms Breast Diseases Skin Diseases Letrozole Palbociclib Antineoplastic Agents Aromatase Inhibitors |
Steroid Synthesis Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Estrogen Antagonists Hormone Antagonists Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs Protein Kinase Inhibitors |