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A Study to Assess the Safety, Tolerability and Pharmacokinetics of BSG005. | Clinical Trials | Clareo Health

UNKNOWNPHASE1

A Study to Assess the Safety, Tolerability and Pharmacokinetics of BSG005.

A Phase 1, Double-blinded, Placebo-controlled Study to Assess the Safety, Tolerability, and Pharmacokinetics of BSG005 Following Single and Multiple Ascending Doses in Healthy Subjects

NCT04921254•Biosergen AS

View on ClinicalTrials.gov

Summary

A Phase 1, double-blinded, placebo-controlled study to assess the safety, tolerability, and pharmacokinetics of BSG005 following single and multiple ascending doses in healthy subjects. The study will include a single ascending dose part and a multiple ascending dose part

Detailed Description

The study will investigate the safety and tolerability of BSG005 in healthy subjects. The study will also include pharmacokinetic investigations. There will be an ascending single dose part (SAD) with 6 subject in a study dose cohort of which 2 will be placebo and 4 will be on active drug. This concept will be replicated in the multiple ascending dose (MAD) part. There is expected to be up to6 cohorts in SAD part with a starting dose calculated from the GLP NOAEL dose levels and from that increasing dose levels will be tested after a Safety Review Committee (SRC) has approved the escalation to next dose level. The key parameters are infusion reactions, kidney, liver and potassium changes during and after administration of BSG005. Depending on the outcome of the SAD part the MAD part may include 4 or 5 dose levels administered daily over 7 days. Key parameters are the same as in the SAD part but extended to cover monitoring over 14 days. Pharmacokinetics at day 1 and day 7 will be investigated. Key evaluation is on safety and tolerability during and after 7 days of dosing and pharmacokinetic investigations and the steady state plasma levels.

Eligibility

Age

18 - 55 years

Sex

MALE

Healthy Volunteers

Yes

Inclusion Criteria

•To be included in this study, each individual must satisfy all the following criteria:
•1. Male adult subjects aged 18 - 55 years at screening.
•2. Subjects without concurrent illnesses who do not require any medical treatments.
•3. Judged by an Investigator to be in good health as documented by the medical history, physical examination (including but may not be limited to an evaluation of the cardiovascular, gastrointestinal, respiratory, and central nervous systems), 12-lead ECG, vital sign assessments, clinical laboratory assessments, and by general observations. Any abnormalities or deviations outside the normal ranges for any of clinical testing (laboratory tests, ECG, vital signs) can be repeated at the discretion of the Investigator(s) and/or judged to be not clinically significant for study participation.
•4. Body Mass Index ≥18 and \<30 kg/m2 and a weight of at least 50 kg.
•5. Negative drug and alcohol screen in urine. Negative pregnancy test (females)
•6. Subject is a non-smoker or smokes ≤ 10 cigarettes per day (or equivalent).
•7. Must be able and willing to provide written informed consent.
•8. Are willing to remain in the study unit for the entire duration of the treatment period, attend all scheduled visits, and comply with all study procedures.
•9. If sexually active males, must use a condom OR abstinence OR same sex partner OR surgically sterile OR partner is of non-childbearing potential.

Exclusion Criteria

•If an individual meets any of the following criteria, he or she is ineligible for this study:
•1. Participation in any study involving an investigational drug or device within the past 30 days or ongoing participation in a study with an investigational drug or device.
•2. Any clinical evidence that the Investigator feels would place the subject at increased risk with the investigational product.
•3. Subject shows clinically significant abnormalities in physical examination, vital signs, 12-lead ECG, or clinical laboratory parameters for the screening assessments (especially for liver enzymes, and serum creatinine and estimated creatinine clearance) according to the Investigator's judgment.
•4. Has liver enzyme results (AST, ALT, GGT) above the upper normal limit (UNL): AST 37 U/L; ALT 78 U/L; GGT 55 U/L.
•5. Has a creatinine value outside the normal range (female \<0.51 mg/dL; male \<0.67 mg/dL) and an estimated creatinine clearance (Cockcroft-Gault) \< 30 mL/min
•6. Subject with, or history of clinically significant neurologic, gastrointestinal, renal, hepatic, cardiovascular, psychological, pulmonary, metabolic, endocrine, hematological, or other major disorders.
•7. Subject who has a sitting or lying blood pressure at screening, after resting for at least 5 minutes: systolic blood pressure \> 155 or \< 90 mmHg, or diastolic blood pressure \> 90 or \< 40 mmHg.
•8. Subject who has a sitting or lying pulse rate at screening, after resting for at least 5 minutes, outside the range of \< 39 or \> 101 beats/min.
•9. Subject who donated blood or who had a comparable blood loss (approximately 500 mL) during the last 30 days prior to start of this study.
+7 more criteria

Locations (1)

Nucleus Network Pty Ltd

Melbourne, Victoria, Australia

Key Dates

Start Date

August 23, 2021

Primary Completion Date

March 1, 2023

Completion Date

May 1, 2023

Last Updated

November 21, 2022

Enrollment

ESTIMATED participants

Conditions

Invasive Fungal Infections

Interventions

BSG005 or placebo

DRUG

Contacts

Peder M Andersen, MD

CONTACT

+45 20802470 peder.andersen@biosergen.net

Tine K Olesen, PhD

CONTACT

+4531355707 Tine.olesen@biosergen.net

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: November 21, 2022Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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A Study to Assess the Safety, Tolerability and Pharmacokinetics of BSG005.

Inclusion Criteria

Exclusion Criteria

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