A Phase 1 interventional study of Testosterone Nasal Gel [Natesto] in Hypogonadism, sponsored by Acerus Biopharma Inc.. Terminated at 3 sites in United Kingdom. Open to male participants aged 12 Years to 17 Years. Per ClinicalTrials.gov, last updated 2023-10-26.
Sponsored by Acerus Biopharma Inc. · Phase 1, Interventional, and Other
PK study to evaluate serum levels of testosterone post nasal delivery in two cohorts of hypogonadal boys.
ARM 1 - 10 prepubertal, 12-17 years old boys with no prior exposure to TRT will receive single dose of 5.5 mg on day one and single dose of 11 mg on day 2 with repeat blood draws to assess serum levels of testosterone and metabolites.
ARM 2 - 10 Tanner Stage 3, 12-17 years old boys on TRT with bone age >= 13 years will receive single dose of 11 mg on day one, and single dose of 11 mg in the morning and a second 11 mg dose in the afternoon on day 2 with repeat blood draws to assess serum levels of testosterone and metabolites.
352 studies on the registry are indexed under Hypogonadism; 44 are open to participants now.
This study's enrollment of 8 is below the median of 55 across 265 interventional studies indexed under Hypogonadism.
Browse Hypogonadism studies →This is the only study on the registry with Acerus Biopharma Inc. as lead sponsor.
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ARM 1 (naïve patients): Participants who meet all of the following inclusion criteria will be eligible for participation in the study:
ARM 2 (non-naïve patients): Participants who meet all of the following inclusion criteria will be eligible for participation in the study:
Exclusion Criteria:
ARM 1 (naïve patients) AND ARM 2 (non-naïve patients): Participants who meet any of the following criteria will be excluded from participation in the study:
TRT naïve subjects, Tanner Stage of 0, receiving Testosterone Nasal Gel \[Natesto\] - Single dose of 5.5 mg Natesto on Day 1 and a single dose of 11 mg Natesto on Day 2
Drug: Testosterone Nasal Gel [Natesto]
TRT non-naïve subjects (have had prior testosterone treatment), Tanner Stage \>/= 3, receiving Testosterone Nasal Gel \[Natesto\] - Single dose of 11 mg Natesto on Day 1. On Day 2, 11 mg dose of Natesto in the morning and 11 mg dose of Natesto 12 hours later
Drug: Testosterone Nasal Gel [Natesto]
nasal gel containing 4.5% w/w testosterone
Maximum plasma concentration (Cmax)
Cmax for serum testosterone, serum DHT and serum estradiol
Time frame: 48 hours (approx)
Area under the curve (AUC)
AUC for serum testosterone, serum DHT and serum estradiol
Time frame: 48 hours (approx)
Minimum serum concentration (Cmin)
Cmin for serum testosterone, serum DHT and serum estradiol
Time frame: 48 hours (approx)
Time to reach maximum plasma concentration (tmax)
tmax for serum testosterone, serum DHT and serum estradiol
Time frame: 48 hours (approx)
Incidence of Treatment-Emergent Adverse Events (Safety)
Safety assessments will include adverse events, clinical laboratory measurements of serum testosterone, DHT and estradiol levels, and vital sign measurements. A phone call will be made 3 days after the patient leaves the clinic to collect any SAEs or AEs that may occur.
Time frame: 5 days
Incidence of Treatment-Emergent Adverse Events (Tolerability)
To include a adverse events that relate to tolerability and a patient and healthcare provider questionnaire on ease of use dispenser and gel administration
Time frame: 48 hours (approx)
Plan to share: No
No publications or documents are linked to this record.
Ran from Mar 2018 to primary completion in Apr 2020, 25 months.
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This study is terminated, as verified in Oct 2023. You cannot join it, but the record below documents what was studied.
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Studies of the drug tested here: Natesto