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Description of Relugolix Use in Patients With Prostate Cancer Within the VHA

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Pfizer

Status

Completed

Conditions

Prostate Cancer

Treatments

Drug: Relugolix

Study type

Observational

Funder types

Industry

Identifiers

NCT06462014
VHA Study (Other Identifier)
C4751009

Details and patient eligibility

About

The purpose of this real-world study is the learn about the demographics and clinical characteristics of patients with prostate cancer who initiated relugolix

Full description

Prostate cancer (PC) is the most common cancer and the second leading cause of cancer death among men in the United States. Androgen deprivation therapy (ADT) such as injectable luteinizing hormone-releasing hormone (LHRH) agonists (e.g., leuprolide) is the standard of care for PC patients. ADT treatment can suppress testosterone level to castrate level and delay the progression of the disease.

Relugolix is a recently approved oral GnRH antagonist. While the introduction of relugolix has offered a unique opportunity for patients with PC, it's vital to understand how it is being used in real-world.

Enrollment

507 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male with ≥ 1 diagnosis for PC
  • Had ≥ 2 prescriptions of relugolix on or after the first observed PC diagnosis.
  • Index date: the initiation date of relugolix
  • At least 18 years old at the index date

Exclusion criteria

  • had surgical castration (bilateral orchiectomy) any time before the index date

Trial design

507 participants in 1 patient group

Relugolix patients
Description:
Patients who have initiated relugolix
Treatment:
Drug: Relugolix

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Pfizer CT.gov Call Center

Data sourced from clinicaltrials.gov

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