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CompletedNCT02460146Updated May 3, 2016

PK and PD of Sequential Multiple Ascending, Repeat Doses of Oral CXA-10 in Healthy Obese Male Subjects

A Phase 1 interventional study of CXA-10 and CXA-10 placebo in Acute Kidney Injury, sponsored by Complexa, Inc.. Completed at 1 site in United States. Open to male participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-05-03.

Sponsored by Complexa, Inc. · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
43
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
Male
01

Study summary

The main purpose of this trial is to demonstrate the safety, tolerability and pharmacokinetics (PK) of CXA-10 and its metabolite(s) administered as multiple ascending oral doses over 14 days to healthy obese male volunteers.

Read the detailed description

Complexa has developed an oral formulation of CXA-10. The main purpose of this trial is to demonstrate the safety, tolerability and pharmacokinetics (PK) of CXA-10 and its metabolite(s) administered as multiple ascending oral doses over 14 days to healthy obese male volunteers. The pharmacodynamic (PD) effects of CXA-10 on serum biomarkers, some of which are elevated in the obese population, will also be investigated.

02

Conditions studied

  • Acute Kidney Injury

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03

In context

Acute Kidney Injury

1,595 studies on the registry are indexed under Acute Kidney Injury; 370 are open to participants now.

This study's enrollment of 43 is below the median of 100 across 763 interventional studies indexed under Acute Kidney Injury.

Browse Acute Kidney Injury studies →

Lead sponsor

Complexa, Inc. is the lead sponsor of 8 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Body mass index (BMI) >27 and ≤40 kg/m2
  • In good general health as determined by a thorough medical history and physical examination, ECG, vital signs, and clinical laboratory evaluation
  • Results of clinical laboratory tests must be without clinically significant abnormalities for this population and may exceed the limits of the reference ranges, including hematology, clinical chemistry and urinalysis except as noted below
  • Hemoglobin A1c (HbA1c) \<7%
  • Average blood pressure \<160/100 mmHg at screening
  • QTcF interval (Fredericia's correction factor) must be ≤430 msec at screening and pre-dose

Exclusion criteria

Exclusion Criteria:

  • Any clinically relevant abnormality for this population identified on the screening history, physical or laboratory examinations, or any other medical condition or circumstance making the volunteer unsuitable for participation in the study
  • Any clinical history of cardiovascular events, arrhythmias, fainting, palpitations, personal or family history of congenital prolonged QT syndromes or sudden unexpected death due to a cardiac reason
  • History of any primary malignancy, including a history of melanoma or suspicious undiagnosed skin lesions, with the exception of basal cell or squamous cell carcinomas of the skin or cervical carcinoma in situ or other malignancies curatively treated and with no evidence of disease for at least 5 years
  • History of regular alcohol consumption exceeding 21 units/week (one unit = 125 mL of wine or 284 mL of beer or a single 25 mL measure of spirits) within 6 months of screening
  • Treatment with any prescription or non-prescription drugs (including vitamins, herbal and dietary supplements) within 7 days or 5 half-lives, whichever is longer, prior to dosing and until collection of the final PK sample. Use of any drug including aspirin or non-steroidal anti-inflammatory drugs (NSAIDs) must be avoided within 7 days prior to the first dose and during this study as it may interfere with the pharmacology of CXA-10. Use of high energy supplements or drinks (especially, those containing caffeine, protein supplements, and weight loss drugs)
  • History of smoking, including e-cigarettes, or use of nicotine-containing products within 1 month of screening
  • Resting heart rate ≥100 BPM after 5 minutes rest (as above) at the screening visit
  • Subjects with any other clinically relevant ECG parameter abnormality (e.g., PR interval, QRS deviation) or any clinically significant ECG abnormality will be excluded from the study
  • Any clinically significant murmurs evident on auscultation of the heart (including evidence of mitral valve prolapse)
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
43 participants (actual)

Study arms

  • Active comparator
    CXA-10

    CXA-10 (10-nitro-9(E)-octadec-9-enoic acid) is a specific isomer of nitrated oleic acid

    Drug: CXA-10

  • Placebo comparator
    CXA-10 placebo

    The placebo contains olive oil with BHT (0.08% to 0.10%).

    Other: CXA-10 placebo

Interventions

  • DrugCXA-10

    CXA-10 (10-nitro-9(E)-octadec-9-enoic acid) is a specific isomer of nitrated oleic acid

  • OtherCXA-10 placebo

    The placebo contains olive oil with BHT (0.08% to 0.10%).

06

What researchers measure

Primary outcomes

  1. Safety (adverse events) and tolerability of multiple ascending oral doses of CXA 10 administered daily for 14 days

    Time frame: 14 days

07

Study locations

1 site
  • Jasper Clinical Research & Development, Inc.
    Kalamazoo, Michigan 49007, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 3, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02460146
Lead sponsor
Complexa, Inc.
Responsible party
Sponsor
First posted
Jun 2, 2015
Start date
Apr 2015
Primary completion
Sep 2015
Completion
Oct 2015
Last update
May 3, 2016

Study contacts

Thomas Blok, MD
principal investigator · Jasper Clinic, Michigan

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2016. You cannot join it, but the record below documents what was studied.

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