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Influence of Administration Route of Testosterone on Male Fertility

Influence on Human Male Fertility of Testosterone After Intranasal (MPP10) or Transdermal (AndroGel™) Application

Status
Withdrawn
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00705796
Enrollment
0
Registered
2008-06-26
Start date
Unknown
Completion date
Unknown
Last updated
2018-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypogonadism

Keywords

Hypogonadism, Spermatogenesis, Quality of Life

Brief summary

Exogenously administered testosterone will override the normal negative feedback of endogenous testosterone on the hypothalamus and pituitary. Constantly, relatively high and constant testosterone levels will cause a drop in FSH and LH production by the pituitary. Since FSH and LH are signalling hormones to the testes, endogenous testosterone production and spermatogenesis will be down-regulated. It is expected that intranasal dosing in the morning will mimic the normal physiological pattern of testosterone production thereby avoiding negative side-effects on spermatogenesis. Trans-dermal gels give testosterone levels more or less constant over the day and will very likely have inhibitory effects on spermatogenesis. The main objective of this study is to show that twice daily intranasal dosing does not have, or has a smaller inhibitory effect on spermatogenesis in comparison to transdermal testosterone gels.

Interventions

DRUGMPP10, testosterone

Testosterone intranasal, 7.6 mg, twice daily to be taken immediately after waking up and washing/showering (approx. 7:00-8:00 AM) and at lunch time (approx. 12:00 AM).

DRUGTestosterone

AndroGel® 50 mg, once daily in the morning after washing/showering.

Sponsors

Acerus Pharmaceuticals Corporation
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
50 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Age greater than or equal to 50 years but not older than 80 years of age; * Serum testosterone level \<13.8 nmol/l; * Sperm concentration \> 40 Million/ml; * Willing to give written informed consent.

Exclusion criteria

* Testicular diseases or having had any surgical procedures applied to the testes; * History or currently existing serious disease of any type, in particular liver, kidney or heart disease, any form of diabetes mellitus, cancer or psychiatric illness; * Current androgen, anabolic steroid or sex hormone treatment or any treatment with such compounds in the previous 6 months; * Blood donation within the 12-week period before the initial study dose. * History of, or current nasal disorders (e.g. seasonal or perennial allergic rhinitis, atrophic rhinitis, polyposis, abuse of nasal decongestants, clinically relevant nasal septum deviation, recurrent epistaxis) or sleep apnea; * Elevated serum PSA levels (\> 4 ng/ml for subjects \>= 50 years of age);

Design outcomes

Primary

MeasureTime frame
The main study parameter is the change in sperm concentration during the 4-month study period for each of the two treatment groups.4 months

Secondary

MeasureTime frame
The effects of treatment on the health related quality of life (QoL);4 months
The influence of transdermal and intranasal testosterone treatment on morphology and motility on sperm cells and on the volume of the ejaculate;4 months

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026