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Completed

NCT Number: NCT03194139

A Study Designed to Compare the Safety and Pharmacokinetics of Intravenously Administered Superoxide Dismutase Mimetic GC4711 and GC4419 in Healthy Volunteers

The study will be a double-blind, randomized, crossover, single-dose assessment of IV-administered GC4711 compared to GC4419 in healthy volunteers.

Consenting subjects will undergo screening procedures within 28 days of the start of dosing. Pharmacokinetics (parent drug and major metabolites) will be assessed in plasma and urine from all subjects.

Initially, a sentinel cohort of 4 subjects, will be enrolled; each eligible subject will receive single dose of GC4711 IV at dose of 30 mg over one hour. Following a clinical safety review by the Galera study team , if no safety concerns are identified after the last subject completes study participation, enrollment will continue in 2 stages to a crossover study design. In stage 1, 12 subjects will be enrolled and in stage 2, if no safety concerns are identified in stage 1 following a clinical safety review by the Galera study team, 20 subjects will be enrolled. In both enrollment stages, eligible subjects in the crossover design will be randomized in 1:1 ratio to one of two treatment sequences: Test (GC4711) -> Ref (GC4419) or Ref (GC4419) -> Test (GC4711). On Day 1, subjects will receive the first treatment they were randomized to, and on Day 4 (following a washout), they will receive the second treatment. Subjects will be followed up for 2 days after the second treatment.

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Key information

Conditions

Healthy Volunteers Healthy

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Nucleus Network Limited

Melbourne, Victoria, 3004, Australia

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy men and women between 18 and 50 years (inclusive) of age;
  • Subjects who provide written informed consent to participate in the study
  • Body Mass Index (BMI) 18 to 32 kg/m2 (inclusive) and weighing at least 50 kg during Screening and at Baseline.
  • Subjects in general good health
  • Chest X-ray free of clinically significant abnormalities
  • Blood pressure and heart rate within normal limits
  • Female subjects must:
  • Have a negative pregnancy test during Screening and Baseline
  • Be non-lactating
  • Be at least two years postmenopausal, surgically sterile or practicing effective contraception

Exclusion criteria

  • History of clinically significant illness, disease, medical condition, or laboratory abnormality
  • Known hypersensitivity and/or allergy to study drugs
  • Use of any prescription or over-the-counter medication within one week prior to baseline;
  • Anticipated need for any medication during the course of the study
  • Use of nitrates or erectile dysfunction drugs such as phosphodiesterase type 5 (PDE 5) inhibitors (e.g., sildenafil, tadalafil, or similar agents), from 24 hours prior to screening throughout participation in the study;
  • Use of or other drugs that may, in the judgment of the treating investigator, create a risk for a precipitous decrease in blood pressure, from 24 hours prior to screening throughout participation in the study;
  • Use of any vitamin or mineral supplement 24 hours prior to dosing, or anticipated use of any vitamin or mineral supplement throughout the duration of the study;
  • Positive HIV, Hepatitis B or Hepatitis C
  • Known history of substance abuse, drug addiction, or alcoholism within 3 years prior to Baseline;
  • Anticipated inability to abstain from alcohol, tobacco, or caffeine use from 48 hours prior to the administration of study drug and throughout the duration of the study;
  • History of smoking or any use of a tobacco product within six months prior to Baseline;
  • Donation of blood or blood products within 30 days prior to the Baseline;
  • Receipt of an investigational test substance within three months prior to the first dose of study drugs or anticipated receiving any study drugs (including placebo on another investigational study)
  • Subject has previously participated in this study, or in a prior study of GC4419 or GC4702.

Treatment and study plan

GC4711 30 mg IV

Drug

GC4711 will be infused IV as a single dose of 30 mg (3 mL GC4711 at 10 mg/mL) in 245 mL normal saline, totaling 250 mL, over a 60-minute period using a programmable pump

GC4711 50 mg IV

Drug

GC4711 will be infused IV as a single dose of 50 mg (5 mL GC4711 at 10 mg/mL) in 245 mL normal saline, totalling 250 mL, over a 60-minute period using a programmable pump.

GC4419 45 mg IV

Drug

GC4419 will be infused IV as a single dose of 45 mg (5 mL GC4419 at 9 mg/mL) in 245 mL normal (0.9%) saline, totalling 250 mL, over a 60-minute period using a programmable pump.

Primary outcomes

  1. Frequency, duration, and severity of adverse events (AEs)

    Time frame: From first dose of study medication until up to 3 days post last dose. Up to 6 days total

  2. Incidence of clinically significant laboratory abnormalities

    Time frame: From first dose of study medication until up to 3 days post last dose. Up to 6 days total

Sponsors and collaborators

Lead sponsor

Galera Therapeutics, Inc.

Industry

Collaborators

  • Syneos Health

Registry information

Official study title

A Phase 1, Randomized, Double-Blind, Crossover, Single Dose Study Designed to Compare the Safety and Pharmacokinetics of Intravenously Administered Superoxide Dismutase Mimetic GC4711 and GC4419 in Healthy Volunteers

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Jun 21, 2017
Registry last updated
Feb 14, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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