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The Role of Follicle Stimulating Hormone in Advanced Prostate Cancer

Primary Purpose

Prostate Cancer Recurrent

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Degarelix 120 MG [Firmagon]
Gonal F RFF Pen 900 UNT Per 1.5 ML Pen Injector
Testosterone Undecanoate
Sponsored by
Lund University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Prostate Cancer Recurrent

Eligibility Criteria

20 Years - 30 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria: Healthy, non-smoking, body mass index 20-25, Exclusion Criteria: Medication or drug abuse

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Sites / Locations

  • Reproductive Medicine Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

GnRH antagonist + FSH + testosterone

GnRH antagonist + testosterone

Arm Description

At the start of the study: 240 mg of the gonadotropin releasing hormone antagonist Degarelix (Ferring GmbH, Wittland, Kiel, Germany) + recombinant FSH (Gonal-f, Merck Serrono S.A. Aubonne, Schweiz), 300 IU every second day for 5 weeks. After 3 weeks: 1000 mg testosterone once.

At the start of the study: 240 mg of the gonadotropin releasing hormone antagonist Degarelix (Ferring GmbH, Wittland, Kiel, Germany). After 3 weeks: 1000 mg testosterone (Nebido, Bayer AB, Solna, Sweden) once.

Outcomes

Primary Outcome Measures

PSA-concentration
Prostate marker

Secondary Outcome Measures

FSH dependent proteins
Proteins identified by spectrophotometry

Full Information

First Posted
October 18, 2019
Last Updated
January 21, 2020
Sponsor
Lund University
Collaborators
Swedish Cancer Foundation, ALF Swedish Government Grant
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1. Study Identification

Unique Protocol Identification Number
NCT04134130
Brief Title
The Role of Follicle Stimulating Hormone in Advanced Prostate Cancer
Official Title
Case Control Study Regarding the Role of Follicle Stimulating Hormone in Chemically Castrated Young Men
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
September 16, 2019 (Actual)
Primary Completion Date
December 20, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lund University
Collaborators
Swedish Cancer Foundation, ALF Swedish Government Grant

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In order to elucidate if FSH can have testosterone like effects, samples from young, non-smoking healthy volunteers, with normal body mass index, and with pharmacologically induced gonadotropin deficiency will be studied regarding their capacity to induce prostate specific antigen (PSA), which normally is regulated by testosterone.
Detailed Description
Normally, prostate specific antigen (PSA), which is a marker for prostate disease and progression, is exclusively produced in response to testosterone. In order to elucidate if follicle stimulating hormone (FSH) can have testosterone like effects, samples from n=30 non-smoking healthy volunteers, 20-30 years of age and with normal body mass index (20-25) with pharmacologically induced gonadotropin deficiency will be studied. The men are currently recruited and during 5 weeks undergoing: Pharmacologically induced gonadotropin deficiency w 1-3; FSH-treatment of 50% (group A), w 1-5; Testosterone (T) treatment of all (group A and B) w 4-5; End and follow up after 5 weeks. A subcutaneous injection with the GnRH antagonist degarelix (240 mg¸ Ferring GmbH Wittland, Kiel, Germany) results in drop of both FSH and LH-induced testosterone. Half of the men will get recombinant FSH (300 IU; Gonal-f, Merck Serrono S.A. Aubonne, Schweiz) back, whereas 50% will not. Three weeks thereafter, the full spectrum of FSH dependent changes occur and are reflected in blood. From this occasion testosterone (Nebido, Ferring GmbH Wittland, Kiel, Germany) will be given to all participants to diminish the side-effects of the castration. Blood samples are collected at start, after 3 wks and after 5 wks. At that point also a follow up is undertaken. This experimental design will provide samples from each individual during normal conditions, during castration, and after a standardised dose of FSH.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer Recurrent

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized case control study: one arm with FSH treatment for 5 weeks and one arm without FSH.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
33 (Actual)

8. Arms, Groups, and Interventions

Arm Title
GnRH antagonist + FSH + testosterone
Arm Type
Other
Arm Description
At the start of the study: 240 mg of the gonadotropin releasing hormone antagonist Degarelix (Ferring GmbH, Wittland, Kiel, Germany) + recombinant FSH (Gonal-f, Merck Serrono S.A. Aubonne, Schweiz), 300 IU every second day for 5 weeks. After 3 weeks: 1000 mg testosterone once.
Arm Title
GnRH antagonist + testosterone
Arm Type
Other
Arm Description
At the start of the study: 240 mg of the gonadotropin releasing hormone antagonist Degarelix (Ferring GmbH, Wittland, Kiel, Germany). After 3 weeks: 1000 mg testosterone (Nebido, Bayer AB, Solna, Sweden) once.
Intervention Type
Drug
Intervention Name(s)
Degarelix 120 MG [Firmagon]
Other Intervention Name(s)
Firmagon
Intervention Description
Two doses of degarelix, 240 mg, subcutaneously once, at study start.
Intervention Type
Drug
Intervention Name(s)
Gonal F RFF Pen 900 UNT Per 1.5 ML Pen Injector
Other Intervention Name(s)
Gonadotropin
Intervention Description
Gonal-f 300 IU subcutaneously 3 times per week for 5 weeks.
Intervention Type
Drug
Intervention Name(s)
Testosterone Undecanoate
Other Intervention Name(s)
Nebido
Intervention Description
One dose 1000 mg testosterone once, after 3 weeks.
Primary Outcome Measure Information:
Title
PSA-concentration
Description
Prostate marker
Time Frame
5 weeks
Secondary Outcome Measure Information:
Title
FSH dependent proteins
Description
Proteins identified by spectrophotometry
Time Frame
5 weeks

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy, non-smoking, body mass index 20-25, Exclusion Criteria: Medication or drug abuse -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yvonne Lundberg Giwercman, Professor
Organizational Affiliation
Lund University, dept Translational medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Reproductive Medicine Center
City
Malmö
ZIP/Postal Code
21428
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Role of Follicle Stimulating Hormone in Advanced Prostate Cancer

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