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Clinical Trials/NCT02381288
NCT02381288
Terminated
Phase 2

A Randomized, Single-Blind, Placebo-Controlled Phase 2a Study to Evaluate the Stimulatory Effects of TAK-448, a Kisspeptin Analog, Administered Intermittently in Middle-aged and Older Men With Low Testosterone

Takeda0 sites17 target enrollmentSeptember 10, 2015

Overview

Phase
Phase 2
Intervention
TAK-448
Conditions
Low Testosterone
Sponsor
Takeda
Enrollment
17
Primary Endpoint
Percent Change From Baseline in Average Serum Concentration (Cav) of Total ST After 6 Weeks of Dosing
Status
Terminated
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the effects on serum testosterone (ST) after 6 weeks of subcutaneous (SC) administration of different doses and dosing frequencies of TAK-448 to middle-aged and older men with low ST levels.

Detailed Description

The drug tested in this study is called TAK-448. TAK-448 was tested to define a dose and dose frequency which results in a clinically relevant improvement in ST in middle-aged and older men with low ST levels. This study looked at ST levels in men who took TAK-448. The study enrolled 17 participants. Participants were randomly assigned (by chance, like flipping a coin) to one of the following treatment groups-which remained undisclosed to the participants and study doctor during the study (unless there is an urgent medical need): * TAK-448 0.1 µg * TAK-448 0.3 µg * TAK-448 1.0 µg * Placebo (dummy inactive injection) - this was a injection that looks like the study drug but has no active ingredient All participants received subcutaneous injection either once daily on Days 1 through 42, or twice weekly on Days 1 through 39 or once weekly on Days 1 through 36. This single-center trial was conducted in the United States. The overall time to participate in this study is up to 56 days. Participants made daily visits to the clinic for 8 weeks, and were contacted by telephone 14 days after last dose of study drug for a follow-up assessment.

Registry
clinicaltrials.gov
Start Date
September 10, 2015
End Date
April 8, 2016
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Sponsor
Takeda
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Has total serum testosterone (ST) levels less than 300 ng/dL at Screening.
  • Has a body mass index (BMI) between 20.0 and 40.0 kg/m\^2, inclusive at Screening.
  • A male participant who is nonsterilized and sexually active with a female partner of childbearing potential agrees to use adequate contraception from the time of signing of informed consent throughout the duration of the study and for 12 weeks after the last dose.

Exclusion Criteria

  • Has uncontrolled, clinically significant neurologic, cardiovascular, pulmonary, hepatic, renal, metabolic, gastrointestinal, or endocrine disease or other abnormality that may impact the ability of the participant to participate or potentially confound the study results. Participants will be excluded based on:
  • Has a serum creatinine \>2.0 milligrams per deciliter (mg/dL) at Screening.
  • Is receiving dialysis treatment.
  • Has an American Urological Association (AUA)/ International Prostate Symptom Score (I-PSS) score of \>19 or serum prostate-specific antigen (PSA) \>4 nanogram per milliliter (ng/mL) at Screening.
  • Has thyrotropin (TSH) levels less than (\<) 0.3 or \>7.5 milli-international units per liter (mIU/L) at Screening.
  • Has systolic blood pressure \>160 millimeter of mercury (mm Hg) or diastolic blood pressure \>100 mm Hg (if out of range may be repeated once for eligibility determination) at Screening.
  • Has luteinizing hormone (LH) \>9.4 units per liter (U/L) at Screening.
  • Is receiving insulin therapy.
  • Has a hematocrit \<30 percent (%) or \>48% at Screening.
  • Has a glycosylated hemoglobin (HbA1c) \>8.0 at Screening (Cohort 1).

Arms & Interventions

TAK-448 0.1 mcg

TAK-448 0.1 mcg, injection, subcutaneously, once daily on Days 1 through 42.

Intervention: TAK-448

TAK-448 0.3 mcg

TAK-448 0.3 mcg, injection, subcutaneously, twice-weekly on Days 1 through 39.

Intervention: TAK-448

TAK-448 1.0 mcg

TAK-448 1.0 mcg, injection, subcutaneously, once-weekly on Days 1 through 36.

Intervention: TAK-448

Placebo

TAK-448 placebo matching injection, subcutaneously, either once daily on Days 1 through 42, or twice weekly on Days 1 through 39 or once weekly on Days 1 through 36.

Intervention: TAK-448

Placebo

TAK-448 placebo matching injection, subcutaneously, either once daily on Days 1 through 42, or twice weekly on Days 1 through 39 or once weekly on Days 1 through 36.

Intervention: TAK-448 Placebo

Outcomes

Primary Outcomes

Percent Change From Baseline in Average Serum Concentration (Cav) of Total ST After 6 Weeks of Dosing

Time Frame: Once-daily regimen Day 42; Twice-weekly regimen Day 39; Once-weekly regimen Day 36

Cav is the average serum concentration of the dosing interval, calculated as area under the effect curve (AUEC) divided by the duration of the dosing interval.

Trough Serum Concentration (Ctrough) of ST

Time Frame: Once-daily regimen Day 42; Twice-weekly regimen Day 39; Once-weekly regimen Day 36

Trough serum concentration of total and free ST, defined as lowest Baseline concentration.

Secondary Outcomes

  • Terminal Elimination Half-life (T1/2) for TAK-448F(Once-daily Dosing Days 1 and 42, Twice-weekly Dosing Days 1 and 39, Once-weekly Dosing Days 1 and 36, predose and at multiple time intervals (up to 8 hours) post-dose.)
  • Serum Testosterone Cmax: Maximum Observed Plasma Concentration(Day 1 (first dose) and Day 42 for once-daily regimen, Day 39 for twice-weekly regimen, or Day 36 for once-weekly regimen (last dose))
  • Cmax: Maximum Observed Plasma Concentration for the Free Form of TAK-448 (TAK-448F)(Once-daily Dosing Days 1 and 42, Twice-weekly Dosing Days 1 and 39, Once-weekly Dosing Days 1 and 36, predose and at multiple time intervals (up to 8 hours) post-dose.)
  • AUCt: Area Under the Plasma Concentration-Time Curve for TAK-448F(Once-daily Dosing Days 1 and 42, Twice-weekly Dosing Days 1 and 39, Once-weekly Dosing Days 1 and 36, predose and at multiple time intervals (up to 8 hours) post-dose.)

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