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CompletedNCT00749788Updated Feb 4, 2013

Efficacy and Safety Study of JTT-302 in Subjects With Low HDL-C Levels

A Phase 2 interventional study of JTT-302 and JTT-302 in Dyslipidemia, sponsored by Akros Pharma Inc.. Completed at 1 site in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2013-02-04.

Sponsored by Akros Pharma Inc. · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
150
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

The purpose of this study is to determine the effect of JTT-302 on the increase of High Density Lipoprotein-Cholesterol (HDL-C) levels when administered daily for four weeks in subjects with low HDL-C levels.

02

Conditions studied

  • Dyslipidemia

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03

In context

Dyslipidemias

1,073 studies on the registry are indexed under Dyslipidemias; 158 are open to participants now.

This study's enrollment of 150 is above the median of 99 across 842 interventional studies indexed under Dyslipidemias.

Browse Dyslipidemias studies →

Lead sponsor

Akros Pharma Inc. is the lead sponsor of 25 studies on the registry; none are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 4 (80%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Subjects with a Body Mass Index (BMI)≤ 35 kg/m2
  • Subjects with the following lipid parameters at Visit 1 (screening visit) and Visit 3 (diet stabilization period):
  • HDL-C ≤ 40 mg/dL (Men) and ≤ 50 mg/dL (Women)
  • TG ≤ 500 mg/dL
  • LDL-C ≤ 190 mg/dL
  • Subjects who are generally healthy as determined by pre-study medical history, physical examination, vital signs and 12-lead ECG

Exclusion criteria

Exclusion Criteria:

  • Females who are pregnant or breast-feeding
  • AST, ALT or total bilirubin ≥ 2.0 x ULN at Visit 1 (screening visit) or Visit 3 (diet stabilization period)
  • Serum thyroid stimulating hormone (TSH) and levothyroxine (T4) outside of the central laboratory reference range at the screening visit
  • Medical history of diabetes mellitus or two fasting serum glucose measurements > 126 mg/dL at the screening visit
  • Subjects with hypertension, or two blood pressure measurements ≥ 140 mm Hg systolic or ≥ 90 mm Hg diastolic at the screening visit
  • History of drug or alcohol abuse within 12 months of the screening visit
  • Use of medications defined in the protocol within six-weeks prior to the screening visit and throughout the study
  • Use of Cytochrome P450 3A4 inducers or inhibitors, as defined in the protocol within four weeks of the screening visit and throughout the study
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
150 participants (actual)

Study arms

  • Experimental
    1

    JTT-302, 200 mg

    Drug: JTT-302

  • Experimental
    2

    JTT-302, 400 mg

    Drug: JTT-302

  • Placebo comparator
    3

    Matching placebo tablets

    Drug: Placebo

Interventions

  • DrugJTT-302

    JTT-302, 100 mg tablets, 200 mg dose, oral, 30 minutes after the start of the morning meal

  • DrugJTT-302

    JTT-302, 100 mg tablets, 400 mg dose, oral, 30 minutes after the start of the morning meal

  • DrugPlacebo

    Matching placebo tablets, oral, 30 minutes after the start of the morning meal

06

What researchers measure

Primary outcomes

  1. Percent change from baseline in HDL-C at Week 4

    Time frame: 4 weeks

Secondary outcomes

  1. Percent change and change from baseline at week 4 in lipid parameters

    Time frame: 4 weeks

  2. Evaluate the safety profile of JTT-302 when administered for 4 weeks

    Time frame: 4 weeks

07

Study locations

1 site
  • Santa Ana, California, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 4, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00749788
Lead sponsor
Akros Pharma Inc.
Responsible party
Sponsor
First posted
Sep 9, 2008
Start date
Dec 2006
Primary completion
Feb 2008
Completion
Feb 2008
Last update
Feb 4, 2013

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2013. You cannot join it, but the record below documents what was studied.

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