Drug-Drug Interaction (DDI) Study in Healthy Volunteers
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|ClinicalTrials.gov Identifier: NCT04814498|
Recruitment Status : Completed
First Posted : March 24, 2021
Last Update Posted : May 17, 2022
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|Condition or disease||Intervention/treatment||Phase|
|Drug Drug Interaction||Drug: Geneva Cocktail Drug: BLD-0409||Phase 1|
This is a single center, open label study designed to determine the effect of BLD-0409 on the PK of probe substrates and to evaluate the safety and tolerability of BLD-0409 administered alone and co-administered with a cocktail of probe substrates (i.e., Geneva cocktail less fexofenadine) in healthy adult volunteers.
Geneva Cocktail (Less Fexofenadine):
- CYP1A2 Caffeine 50 mg
- CYP2C Flurbiprofen 10 mg
- CYP2C19 Omeprazole 10 mg
- CYP2D6 Dextromethorphan 10 mg
- CYP3A4 Midazolam 1 mg
- CYP2B6 Bupropion 20 mg
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||16 participants|
|Intervention Model:||Sequential Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Phase 1, Open Label, Fixed Sequence Study to Evaluate the Effect of BLD-0409 on the Single Dose Pharmacokinetics of a Cocktail of Probe Substrates for CYP450 Enzymes in Healthy Volunteers|
|Actual Study Start Date :||May 3, 2021|
|Actual Primary Completion Date :||September 17, 2021|
|Actual Study Completion Date :||January 11, 2022|
Experimental: Geneva cocktail (less fexofenadine) & BLD-0409
Following an overnight fast of at least 10 hours, subjects will be administered IP in a fixed sequence.
Drug: Geneva Cocktail
Fixed sequence use of drug cocktail
Fixed sequence use of active product
- Area under the drug concentration-time curve from time zero to the last measurable concentration (AUC0-last) [ Time Frame: Up to 16 days ]Measured by plasma concentration of probe substrates
- Maximum observed drug concentration (Cmax) [ Time Frame: Up to 16 days ]Measured by plasma concentration of probe substrates
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|
- Provide signed informed consent prior to study entry.
- Males and females aged 18 to 55 years at the time of consent.
- Body mass index (BMI) ≥ 18 and ≤ 32 kg/m2.
- Agree to abstain from alcohol intake from 48 hours before first IP administration through to discharge from the CRU.
- Agree to abstain from all caffeine- and xanthine-containing products (e.g., coffee, tea, cola drinks, chocolate) for 48 hours before first IP administration through to discharge from the CRU.
- Have a negative urine drug screen/alcohol breath test at Day -1 (Admission). Repeat urine drug screens will be permitted for suspected false positive results.
- Use of acceptable contraception.
- Males must not donate sperm for at least 90 days after the last dose of study drug.
- Females of childbearing potential must have a negative serum pregnancy test at Screening and a negative urine or serum pregnancy test on Day -1. If a urine test is conducted and it is positive, a serum pregnancy test must also be performed for confirmation. Females not of childbearing potential must be postmenopausal (defined as cessation of regular menstrual periods for at least 12 months), confirmed by follicle-stimulating hormone (FSH) level > 40 mIU/mL at Screening.
- In good general health, in the opinion of the Principal Investigator (PI), with no significant medical history, have no clinically significant abnormalities on physical examination at Screening, and/or before administration of the initial dose of study drug.
- Have clinical laboratory values within normal ranges.
- Active smoker and/or user of nicotine-containing products (i.e., have not used nicotine-containing products within the previous 3 months).
- Human immunodeficiency virus (HIV) antibody positive.
- Hepatitis B surface antigen (HBsAg) positive or Hepatitis C virus (HCV) positive.
- Presence of any underlying or clinically significant physical or psychological medical condition (e.g., hypertension, elevated cholesterol/triglycerides, asthma, or diabetes) that, in the opinion of the PI, would make it unlikely that the subject will complete the study per protocol.
- History or presence of alcohol or drug abuse (including recreational marijuana use) within the 2 years prior to the first IP administration, and unwillingness to be totally abstinent during the period of confinement.
- Blood donation or significant blood loss within 30 days prior to the first study drug administration.
- Plasma donation within 7 days prior to the first study drug administration.
- Administration of IP in another trial within 30 days prior to the first IP administration, or 5 half-lives, whichever is longer.
- Females who are pregnant or breastfeeding.
- Surgery within the past 3 months prior to the first IP administration determined by the PI to be clinically relevant.
- Consumption of any nutrients known to modulate cytochrome P450 3A4 (CYP3A4) or any strong inhibitors or inducers of CYP3A4, starting from 14 days prior to the first dose of IP on Day 1 and until the EOS assessments.
- Consumption of cruciferous vegetables or chargrilled meat more than 3 × per week in the previous 2 weeks.
- Inability to refrain from consumption of grapefruit and Seville oranges or St. John's Wort within 14 days prior to the first dose of IP on Day 1 and until the EOS assessments.
- Failure to satisfy the PI of fitness to participate for any other reason.
- Active infection (diagnosed or suspected) or history of recurrent infections.
- Active malignancy and/or history of malignancy in the past 5 years, except for completely excised non-melanoma skin carcinomas or low grade cervical intraepithelial neoplasia.
- Serious local infection or systemic infection within 3 months requiring antibiotic treatment.
- Any acute illness within 30 days prior to Day 1.
- Use of any prescription or over-the-counter (OTC) medication (except for paracetamol and approved contraceptives) within 5 days or 5 half-lives (whichever is longer) prior to dosing and during course of study without prior approval of the Investigator and Medical Monitor. Simple analgesia (paracetamol) may be permitted at the discretion of the Investigator.
- For all participants, the use of any estrogen-containing products (e.g., contraceptives, patch, cream, implants) within 14 days prior to the first study drug administration and until the EOS assessments.
- Inability to refrain from vaccinations within 14 days of the first dose of IP and until the EOS assessments.
- History of allergy or intolerance to any IP or IP constituents used on study or any clinically significant drug allergy as per the PIs judgment.
- History of anaphylaxis or other severe allergic reaction to drug, food, toxin, or other exposure.
- Any surgical or medical condition that could interfere with the absorption, distribution, metabolism, or excretion of the IP.
- Any evidence of cardiac disease or clinically significant abnormalities on ECG.
- Systolic blood pressure (BP) > 150 mmHg or < 80 mmHg or diastolic BP > 90 mmHg or < 50 mmHg at Screening with one repeat allowed per the PIs discretion at Screening and Day -1.
- Heart rate < 40 bpm or > 100 bpm at Screening with one repeat allowed per the PIs discretion at Screening and Day -1.
- Diets that could alter metabolism (i.e., high protein, Slim Fast®, Nutrisystem®, etc.) within 7 days prior to dosing on Day 1.
- Weight loss or gain of ≥ 10% in the 30 days prior to dosing.
- Strenuous exercise, including weightlifting, (> 5 × per week) within 2 weeks prior to first IP administration on Day 1.
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): NCT04814498
|Nucleus Network Pty Ltd.|
|Herston, Queensland, Australia, 4006|
|Principal Investigator:||Kristi McLendon, MD||Nucleus Network|
|Responsible Party:||Blade Therapeutics|
|Other Study ID Numbers:||
|First Posted:||March 24, 2021 Key Record Dates|
|Last Update Posted:||May 17, 2022|
|Last Verified:||May 2022|
|Individual Participant Data (IPD) Sharing Statement:|
|Plan to Share IPD:||No|
|Studies a U.S. FDA-regulated Drug Product:||No|
|Studies a U.S. FDA-regulated Device Product:||No|