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Fulvestrant for the Treatment of Recurrent or Metastatic Endometrial Carcinoma.

AstraZeneca logo

AstraZeneca

Status and phase

Completed
Phase 2

Conditions

Endometrial Carcinoma

Treatments

Drug: Fulvestrant

Study type

Interventional

Funder types

Industry

Identifiers

NCT00334295
9238GR/0002

Details and patient eligibility

About

The purpose of this study is to determine the efficacy of a monthly administration of Fulvestrant in patients with recurrent or metastatic endometrial carcinoma by assessment of the clinical tumour response after 3 injections.

Enrollment

35 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Histologically confirmed, recurrent or metastatic endometrial carcinoma
  • Postmenopausal
  • Hormonreceptor positive

Exclusion criteria

  • Pre-treatment with Fulvestrant
  • Previous endocrine therapy of the endometrial carcinoma
  • Previous malignancy less than 3 years ago other than in situ carcinoma of the cervix, basal cell carcinoma or squamous carcinoma of the skin

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

9

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Data sourced from clinicaltrials.gov

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