Status:
COMPLETED
SAD/MAD Safety and PK Study of QPX9003 (Novel Polymyxin) in Normal Healthy Volunteers
Lead Sponsor:
Qpex Biopharma, Inc.
Collaborating Sponsors:
Biomedical Advanced Research and Development Authority
Conditions:
Bacterial Infections
Eligibility:
All Genders
18-60 years
Phase:
PHASE1
Brief Summary
The worldwide spread of resistance to antibiotics among gram-negative bacteria, particularly members of the ESKAPE group of pathogens, has resulted in a crisis in the treatment of hospital acquired in...
Detailed Description
The United States (US) Centers for Disease Control (CDC) have listed multidrug-resistant (MDR) Acinetobacter and MDR Pseudomonas aeruginosa as serious threats \[CDC, 2019\]. Consistent with the global...
Eligibility Criteria
Inclusion
- Healthy adult males and/or females of non-child bearing potential, 18 to 60 years of age (inclusive).
- Body mass index (BMI) ≥ 18.5 and ≤ 29.9 (kg/m2) and weight between 55.0 and 100.0 kg (inclusive).
- Medically healthy with clinically insignificant screening results (e.g., laboratory profiles, medical histories, electrocardiograms \[ECGs\], physical examination) as assessed by the PI.
- Voluntarily consent to participate in the study.
- If male, agree to be sexually abstinent or agree to use a condom when engaging in any sexual activity from Day -1 check-in to the clinic through 30 days following the last administration of the study drug, and to not donate sperm during this same period of time.. If engaging in sexual activity with a female partner of childbearing potential, an additional method of birth control must be used.
- Approved additional methods of birth control include:
- Intra-uterine device (IUD) in place for at least 3 months prior to Day 1 through 30 days following the final dosing of the study drug.
- Barrier method (diaphragm) for at least 14 days prior to Day 1 through 30 days following the final dosing of the study drug.
- Stable hormonal contraceptive for at least 3 months prior to Day 1 through 30 days following the final dosing of the study drug.
- Surgical sterilization (vasectomy) at least 6 months prior to Day 1.
- Females of non-childbearing potential must meet at least one of the following criteria:
- postmenopausal (defined as 12 months spontaneous amenorrhea) with a serum FSH leve l≥ 40 mIU/mL.
- have undergone one of the following sterilization procedures documented at least 6 months prior to Day 1:
- Bilateral tubal ligation
- Hysterectomy
- Hysterectomy with unilateral or bilateral oophorectomy
- Bilateral oophorectomy
- Females who practice true abstinence or are in same sex relationships where there is no possibility of conception.
- In addition to meeting Inclusion Criteria 1 through 6, cCohort 12 will consist of normal healthy Chinese subjects who are either:
- a. First generation Chinese subjects born in China, with 2 Chinese biological parents and 4 Chinese grandparents born in China of full Chinese descent.
- i. Subject has lived less than or equal to 10 years outside of China. ii. In addition to mainland China, subjects or their parents and grandparents may also be from Taiwan, Hong Kong, or Mongolia, or b. Second generation Chinese subjects born outside of China with 2 Chinese biological parents and 4 grandparents born in China of full Chinese descent.
Exclusion
- History or presence of significant cardiovascular, pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine, immunologic, dermatologic, neurological, or psychiatric disease.
- Positive urine drug screen or alcohol breath test at screening or check-in (Day -1).
- Positive testing for HIV, hepatitis B or C
- History or presence of alcoholism or drug abuse within last 2 years
- Use of more than 5 packs/week of tobacco/nicotine-containing product within last 6 months prior dosing.
- Use of any prescription medication (with the exception of hormonal contraceptives or hormone replacement therapy for females) within 14 days prior to dosing.
- Use of any over-the-counter (OTC) medication, including herbal products, probiotics and vitamins, within the 7 days prior to dosing.
- Use of antacids, H2 receptor blockers or proton pump inhibitors 7 days prior to dosing.
- History of any hypersensitivity reaction or anaphylaxis to any medication, including polymyxin antibiotics.
- Participation in another investigational clinical trial within 30 days prior to Day 1 or within 5 half-lives of the previous investigational drug, whichever is longer.
- Females who are pregnant or lactating.
- QTcF interval \>450 msec for males and \>470 msec for females, or history of prolonged QT syndrome at screening or check-in.
- Calculated creatinine clearance less than 80 mL/min (Cockcroft-Gault method) at screening or check-in.
- Subjects who have any clinically significant abnormalities on laboratory values: White blood cell count \< 3,000/mm3, hemoglobin \< 11g/dL or Absolute neutrophil count \< 1,200/mm3 or platelet count \< 120,000/mm3.
- Liver function abnormalities defined by an elevation in bilirubin, Aspartate Aminotransferase (AST) or Alanine Aminotransferase (ALT) 1.5 x Upper Limit of Normal (ULN) of the normal range for subjects based on age and sex.
Key Trial Info
Start Date :
June 3 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 14 2022
Estimated Enrollment :
104 Patients enrolled
Trial Details
Trial ID
NCT04808414
Start Date
June 3 2021
End Date
July 14 2022
Last Update
October 10 2022
Active Locations (1)
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1
Altasciences
Cypress, California, United States, 90630