Healthy Male Volunteers | First-time-in-man, to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of BP1.5375

Healthy Male Volunteers research study

What is the primary objective of this study?

Phase I Single Ascending Dose (Part 1), phase IIa Proof Of Concept (Part 2)

Who is eligible to participate?

Inclusion Criteria: - Signed informed consent prior to any study-mandated procedure. - Healthy male subjects aged between 18 and 45 years (inclusive). - Subjects with a body weight of at least 50 kg and a body mass index (BMI) between 18.0 and 28.0 kg/m2 (both inclusive). - Healthy subjects, based on history, physical examination, complete laboratory evaluation, and 12-lead ECG. - Normal arterial blood pressure (BP) and pulse rate or, if abnormal, considered not clinically significant by the investigator. Normal BP to be [100-140] mmHg systolic and [45-90] mmHg diastolic. Normal pulse rate to be [40-90] bpm after 5 minutes rest in lying position. Ability to communicate well with the investigator in the local language, and to understand and comply with the requirements of the study. Exclusion Criteria: - Subject with a history of cardiovascular, pulmonary, gastro-intestinal, hepatic, renal, metabolic, haematological, neurological, psychiatric, systemic, or infectious disease, or any other condition which, in the opinion of the investigator, would jeopardize the safety of the subject, or impact the validity of the study results. - Previous history of fainting, collapse, syncope, orthostatic hypotension, or vasovagal reactions. - Haematology, clinical chemistry, and urinalysis results deviating from the normal range to a clinically relevant extent at screening. - Clinically significant findings on physical examination at screening. - 12-lead electrocardiogram (ECG) with clinically relevant abnormalities in supine position at screening. - Positive results from urine drug screen at screening. - Veins unsuitable for i.v. puncture on either arm (e.g., veins that are difficult to locate, access or puncture, or veins with a tendency for rupture during or after puncture). - Treatment with any prescribed medications (including vaccines) or over-the-counter (OTC) medications (including herbal medicines such as St John's Wort) within 2 weeks prior to the (first) scheduled administration of study drug, except paracetamol (maximum 1 g/day). - Treatment with another investigational drug within 3 months prior to screening or having participated in more than four investigational drug studies within 1 year prior to screening. - History or clinical evidence of alcoholism or drug abuse within the 3-year period prior to screening. - History or clinical evidence of any disease, and/or existence of any surgical or medical condition, which might interfere with the absorption, distribution, metabolism or excretion of the study drugs. - Have undergone surgery or have donated an amount equal or more than 500 mL blood, or 300 mL of plasma, within 3 months prior to screening. - Positive results from any of the hepatitis serology tests (HBsAg, anti-HCV), at screening. - Positive results from the HIV 1 or/and 2 serology at screening. - History of allergy to diphenhydramine or antihistaminic drugs. - Smoking more than 5 cigarettes per day.

Which medical condition, disease, disorder, syndrome, illness, or injury is researched?

Healthy Male Volunteers

Study Interventions

Interventions can include giving participants drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available or noninvasive approaches such as surveys, education, and interviews.

Drug:BP1.5375 suspensionsingle oral dose

Drug:Diphenhydraminesingle oral dose of Diphenhydramine 50mg

Drug:PlaceboSingle oral dose

Study Arms

Research studies and clinical trials typically have two or more research arms. An arm is a group of people who receive the same treatment in the study.

BP1.5375Single oral administration ranging from 0.5 mg to 100 mg

DiphenhydramineSingle oral dose of diphenhydramine 50mg

PlaceboSingle oral dose

Study Status


Start Date: October 2014

Completed Date: December 2014

Phase: Phase 1

Type: Interventional


Primary Outcome: Single Ascending Dose - safety and tolerability (Part 1)

Secondary Outcome:

Study sponsors, principal investigator, and references

Principal Investigator: van Gerven Joop, MD

Lead Sponsor: Bioprojet


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