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Trial record 1 of 1 for:    C27005
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A Phase 1 Study to Evaluate the Effects of Fluconazole and Atorvastatin on the Pharmacokinetics of TAK-385 in Healthy Subjects

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT02093390
First Posted: March 21, 2014
Last Update Posted: June 6, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Millennium Pharmaceuticals, Inc.
  Purpose
This is a nonrandomized, open-label, fixed-sequence, 2-arm study designed to assess the effect of multiple doses of fluconazole or atorvastatin on the single-dose pharmacokinetics of TAK-385 in healthy adult subjects.

Condition Intervention Phase
Prostate Cancer Endometriosis Drug: TAK-385 Drug: Fluconazole Drug: Atorvastatin Phase 1

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 1, Open-Label, Drug-Drug Interaction Study to Evaluate the Effects of Multiple Oral Doses of Fluconazole and Atorvastatin on the Pharmacokinetics of a Single Oral Dose of TAK-385 in Healthy Subjects

Resource links provided by NLM:


Further study details as provided by Millennium Pharmaceuticals, Inc.:

Primary Outcome Measures:
  • Cmax: Maximum Observed Plasma Concentration of TAK-385 on Day 1 [ Time Frame: Day 1 (Predose and multiple time points up to 120 hours postdose) ]
    Cmax is the peak concentration of a drug after administration, obtained directly from the plasma concentration-time curve.

  • Cmax: Maximum Observed Plasma Concentration of TAK-385 on Day 10 [ Time Frame: Day 10 (Predose and multiple time points up to 120 hours postdose) ]
    Cmax is the peak concentration of a drug after administration, obtained directly from the plasma concentration-time curve.

  • AUC(0-tlast): Area Under the Plasma Concentration Curve From Time Zero to the Time of the Last Quantifiable Concentration of TAK-385 on Day 1 [ Time Frame: Day 1 (Predose and multiple time points up to 120 hours postdose) ]
    Area under the plasma concentration versus time curve from zero to the time of the last quantifiable concentration.

  • AUC(0-tlast): Area Under the Plasma Concentration Curve From Time Zero to the Time of the Last Quantifiable Concentration of TAK-385 on Day 10 [ Time Frame: Day 10 (Predose and multiple time points up to 120 hours postdose) ]
    Area under the plasma concentration versus time curve from zero to the time of the last quantifiable concentration.

  • AUC(0-inf): Area Under the Plasma Concentration-Time Curve From Time 0 to Infinity of TAK-385 on Day 1 [ Time Frame: Day 1 (Predose and multiple time points up to 120 hours postdose) ]
    Area under the plasma concentration-time curve from time 0 to infinity.

  • AUC(0-inf): Area Under the Plasma Concentration-Time Curve From Time 0 to Infinity of TAK-385 on Day 10 [ Time Frame: Day 10 (Predose and multiple time points up to 120 hours postdose) ]
    Area under the plasma concentration-time curve from time 0 to infinity.


Secondary Outcome Measures:
  • Number of Participants With at Least 1 Treatment Emergent Adverse Event (AE) [ Time Frame: First dose of study drug through the end of the study (22 days ± 3 days) ]
    An Adverse Event (AE) is defined as any untoward medical occurrence in a clinical investigation participant administered a drug; it does not necessarily have to have a causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign (eg, a clinically significant abnormal laboratory finding), symptom, or disease temporally associated with the use of a drug, whether or not it is considered related to the drug. A treatment-emergent adverse event (TEAE) is defined as an adverse event with an onset that occurs after receiving study drug.

  • Number of Participants With Clinical Significant Changes in Vital Signs [ Time Frame: Baseline and First dose of study drug through the end of the study (22 days ± 3 days) ]
    Vital sign measurements included oral temperature, heart rate, supine (after 3 to 5 minutes in this position) and standing (after 3 to 5 minutes in this position) measurements of diastolic and systolic blood pressure.

  • Number of Participants With Clinical Significant Changes in Electrocardiogram (ECG) Findings [ Time Frame: Baseline and First dose of study drug through Day 15 ]
    A 12-lead ECG was administered on Days 1,9,10,11,15.

  • Number of Participants With Clinical Significant Changes in Laboratory Tests [ Time Frame: Baseline and First dose of study drug through the end of the study (22 days ± 3 days) ]
    Blood samples were collected for analysis of clinical chemistry and hematological parameters and urine samples were obtained for urinalysis. Clinical laboratory evaluations were performed at central and /local laboratories.

  • Tmax: Time to Reach the Maximum Plasma Concentration of TAK-385 [ Time Frame: Days 1 and 10 (Predose and multiple time points up to 120 hours postdose) ]
    Tmax is the time to reach the maximum concentrations (Cmax), equal to time (hours) to Cmax.

  • AUC (0-120): Area Under the Plasma Concentration-Time Curve From Time 0 to 120 Hours of TAK-385 [ Time Frame: Days 1 and 10 (Predose and multiple time points up to 120 hours postdose) ]
    Area under the plasma concentration versus time curve from 0 to 120 hours after study drug administration.

  • Terminal Disposition Half-life (t1/2) of TAK-385 [ Time Frame: Days 1 and 10 (Predose and multiple time points up to 120 hours postdose) ]
    Terminal disposition half-life (T1/2) is the time required for half of the drug to be eliminated from the plasma.

  • Apparent Total Body Clearance (CL/F) of TAK-385 [ Time Frame: Days 1 and 10 (Predose and multiple time points up to 120 hours postdose) ]
  • Fraction Excreted Unchanged (Fe) of TAK-385 [ Time Frame: Days 1 and 10 (Predose and multiple time points up to 120 hours postdose) ]
    Fraction of TAK-385 excreted in the urine unchanged.

  • Plasma Trough Concentrations for Fluconazole [ Time Frame: Days 8 to 12 Predose ]
    Blood samples for fluconazole trough levels were collected predose (before dosing with fluconazole and before breakfast) on Days 8 through 12.

  • Plasma Trough Concentrations for Atorvastatin [ Time Frame: Days 8 to 12 Predose ]
    Blood samples for atorvastatin trough levels were collected predose (before dosing with atorvastatin and before breakfast) on Days 8 through 12.


Enrollment: 40
Study Start Date: March 2014
Study Completion Date: April 2014
Primary Completion Date: April 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: TAK-385 + fluconazole
TAK-385 40 mg, tablet, orally once on Day 1 and fluconazole 400 mg, tablet, orally on Day 6 then 200 mg, tablet, orally once daily on Days 7 to 9 followed by a single dose of TAK-385 in combination with fluconazole 200 mg on Day 10 then fluconazole 200 mg, tablet, orally once daily alone on Days 11 to 14.
Drug: TAK-385
TAK-385 tablets
Drug: Fluconazole
Fluconazole tablets
Experimental: TAK-385 + atorvastatin
TAK-385 40 mg, tablet, orally once on Day 1 and atorvastatin 80 mg, tablet, orally once daily on Days 6 to 9 followed by a single dose of TAK-385 in combination with atorvastatin 80 mg on Day 10 then atorvastatin 80 mg, tablet, orally once daily alone on Days 11 to 14.
Drug: TAK-385
TAK-385 tablets
Drug: Atorvastatin
Atorvastatin tablets

Detailed Description:

The drug being tested in this study is called TAK-385. TAK-385 was being tested to assess if the way it is processed the body changes when it administered with other medications (fluconazole or atorvastatin). This study looked at lab results in people who took TAK-385.

The study enrolled 40 patients. Participants were assigned to one of the two treatment groups:

  • TAK-385 40 mg and fluconazole 400 mg on Day 6 and 200 mg on Days 7 to 14
  • TAK-385 40 mg and atorvastatin 80 mg on Days 6-14

Participants in the fluconazole arm were administered TAK-385 on Days 1 and 10 and fluconazole on Days 6 through 14. Participants in the atorvastatin arm were administered TAK-385 on Days 1 and 10 and atorvastatin on Days 6 through 14.

This single-center trial was conducted in the United States. The overall time to participate in this study was 4 weeks. Participants made multiple visits to the clinic, including one 16-day period of confinement to the clinic, and a final visit 7 days after last dose of study drug for a follow-up assessment.

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria

Each subject must meet all the following inclusion criteria to be enrolled in the study:

  1. Age 18 to 55 years, inclusive, at the time of consent.
  2. Healthy adult male or female in good health, as determined by a physician evaluation
  3. Weight ≥ 45 kg and body mass index (BMI) between 18.0 and 30.0 kg/m2, inclusive, at screening.
  4. Nonsmoker and does not use tobacco-containing products (including, but not limited to, cigarettes, pipes, cigars, chewing tobacco, or nicotine patch or gum).

Exclusion Criteria Subjects meeting any of the following exclusion criteria are not to be enrolled in the study.

  1. The subject has a history of drug abuse (defined as any illicit drug use) within 1 year before screening or is unwilling to abstain from drugs throughout the study.
  2. The subject is unwilling to agree to abstain from caffeine and alcohol-containing products from 72 hours before check-in (Day -1) to completion of the final assessment.
  3. The subject has taken any prescription medicine or herbal preparations (eg, St John's wort) or received any immunizations within 30 days before check-in (Day -1).
  4. The subject has taken any over the counter (OTC) medications or vitamin supplements within 14 days before check-in (Day -1). The subject is unwilling to agree to abstain from consumption of grapefruit or grapefruit-containing products from 72 hours before check-in (Day -1) to completion of the final assessment.
  5. The subject has current or recent (within 6 months) history of gastrointestinal disease that would be expected to influence the absorption of drugs.
  6. The subject has a positive test result for hepatitis B surface antigen, hepatitis C virus (HCV) antibody, human immunodeficiency virus (HIV) antibody or antigen, or serological reactions for syphilis at screening.
  7. The subject has a clinically significant ECG abnormality at screening or check-in (Day -1) or a QTc interval (by Fridericia's correction) of 450 msec or greater, or the subject has a history of cardiac disease.
  8. The subject has abnormal laboratory values suggesting a clinically significant disease at screening or check-in (Day -1) .
  9. Female subjects who are lactating and breastfeeding or pregnant before the first dose of study drug.
  10. Any serious medical or psychiatric illness that could, in the investigator's opinion, potentially interfere with the completion of treatment according to this protocol.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02093390


Sponsors and Collaborators
Millennium Pharmaceuticals, Inc.
Investigators
Study Director: Medical Monitor Millennium Pharmaceuticals, Inc.
  More Information

Responsible Party: Millennium Pharmaceuticals, Inc.
ClinicalTrials.gov Identifier: NCT02093390     History of Changes
Other Study ID Numbers: C27005
U1111-1183-0138 ( Registry Identifier: WHO )
First Submitted: March 19, 2014
First Posted: March 21, 2014
Results First Submitted: April 17, 2015
Results First Posted: June 6, 2016
Last Update Posted: June 6, 2016
Last Verified: June 2016

Additional relevant MeSH terms:
Endometriosis
Genital Diseases, Female
Atorvastatin Calcium
Fluconazole
Anticholesteremic Agents
Hypolipidemic Agents
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Lipid Regulating Agents
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Enzyme Inhibitors
Antifungal Agents
Anti-Infective Agents
14-alpha Demethylase Inhibitors
Cytochrome P-450 Enzyme Inhibitors
Steroid Synthesis Inhibitors
Hormone Antagonists
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Cytochrome P-450 CYP2C9 Inhibitors
Cytochrome P-450 CYP2C19 Inhibitors