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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00537836
Other study ID # 91544
Secondary ID 2007-001791-3631
Status Completed
Phase Phase 2
First received September 28, 2007
Last updated April 8, 2015
Start date October 2007
Est. completion date December 2008

Study information

Verified date April 2015
Source Bayer
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Interventional

Clinical Trial Summary

The primary goal of the planned study is to investigate the efficacy and safety of ZK 283197 in the dosage of 2 and 3 mg ingested once daily during a period of 8 weeks for the treatment of hot flushes. In order to be able to assess the efficacy of the test substance, this is compared with the efficacy of 1 mg Estradiol and placebo. The comparator Estradiol is a certified hormone preparation, which is already used for the treatment of hot flushes as standard treatment. After passing the screening, volunteers will start with a run-in phase followed by a 8 weeks treatment and a follow-up phase. 112 postmenopausal women with hot flushes and without relevant prior diseases will participate in three European countries (2 study sites in Germany, 1 study site in Great Britain and 1 study site in The Netherlands) in this study.


Recruitment information / eligibility

Status Completed
Enrollment 116
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Female
Age group 45 Years to 65 Years
Eligibility Inclusion Criteria:

- Women with at least 35 moderate to severe hot flushes in seven consecutive days

- Body mass index (BMI) : 20 - 30 kg/m² (inclusive)

- Postmenopausal status

Exclusion Criteria:

- Contraindication for use for hormonal therapy

- Prior hysterectomy

- Hormonal therapy or intrauterine hormone releasing device within 4 weeks prior to study entry or any long-acting injectable or implant up to 6 months prior to study entry

- Repeated intake of medications affecting study aim

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
BAY 86-5310 (ZK 283197)
3 mg (3 x 1 mg tablet) or 2 mg (2 x 1 mg tablet) ZK 283197 in respective treatment group, once daily p.o. over 8 weeks
Placebo
Placebo, once daily p.o. over 8 weeks
17ß-estradiol
1 mg (2 x 0.5 mg tablet) 17ß-estradiol, once daily p.o. over 8 weeks

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Bayer

Countries where clinical trial is conducted

Germany,  Netherlands,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Relative change in frequency of moderate to severe hot flushes per week between baseline and Week 8 of the treatment phase Between baseline and Week 8 of the treatment phase No
Secondary Number of participants with adverse events From Week 1 of treatment until end of Follow-up period (approximately 12 weeks) Yes
Secondary Exposure-response relationship A generalized linear model was applied to explore the dependence of the number of hot flushes in Week 8 to (i) the dose of ZK 283197, (ii) the AUC of ZK 283197, (iii) the maximum concentration Cmax of ZK 283197 and (iv) the average concentration Cave of ZK 283197 At week 8 No
Secondary Change from baseline to all treatment weeks in frequency and severity of moderate to severe hot flushes From baseline up to 8 weeks No
Secondary Change from baseline to all treatment weeks in severity and frequency of all hot flushes From baseline up to 8 weeks No
Secondary Trough levels at every visit Before 1st administration and at Week 1, 2, 4, 6 and 8 No
Secondary AUC(0-24h) Area under the curve from administration to 24 h after administration Pre-dose and up to 24 h post-dose (measured between Week 4-8) No
Secondary Cmax Maximum serum concentration Pre-dose and up to 24 h post-dose (measured between Week 4-8) No
Secondary tmax Time to reach maximum drug concentration Pre-dose and up to 24 h post-dose (measured between Week 4-8) No
Secondary Cmin Minimum serum concentration Pre-dose and up to 24 h post-dose (measured between Week 4-8) No
Secondary Cave Average serum concentration Pre-dose and up to 24 h post-dose (measured between Week 4-8) No
Secondary Vaginal cytology The epithelial maturation index/value and the karyopycnotic index were assessed Between baseline and Week 8 Yes
Secondary Endometrial thickness Transvaginal ultrasound was performed to demonstrate the absence of relevant endometrium growth Fom baseline to Week 8 Yes
Secondary Endometrial histology Between baseline and Week 8 Yes
See also
  Status Clinical Trial Phase
Completed NCT00369434 - Study of the Safety and Efficacy of Desvenlafaxine Succinate for Vasomotor Symptoms in Postmenopausal Women Phase 3