Evaluating the Safety, Tolerability, and Pharmacokinetics of BIIB095 in Healthy Participants

NCT03454126 | Completed Phase 1

• 2 other identifiers: 255HV1012017-003982-90
• Study Type: interventional
• Target: 80
• Locations: 1 country
• Sites: 2

Brief Summary

The primary objective of the study is to evaluate the safety and tolerability of single- and multiple-ascending oral doses of BIIB095 in healthy participants. The secondary objectives are to characterize the single- and multiple-oral-dose PK of BIIB095 in healthy participants and to investigate the effect of food on the single-oral-dose PK of BIIB095 in healthy participants.

Conditions

Healthy Volunteer

Keywords

Chronic pain; Neuropathic pain; Neuralgia; Healthy volunteers

Outcome Measures

Primary Outcomes (6)

• Percentage of Participants with Serious Adverse Events (SAEs)

  An SAE is any untoward medical occurrence that at any dose: Results in death; in the view of the Investigator, places the participant at immediate risk of death (a life threatening event), however, this does not include an event that, had it occurred in a more severe form, might have caused death; requires inpatient hospitalization or prolongation of existing hospitalization; results in persistent or significant disability/incapacity; results in a congenital anomaly/birth defect; is a medically important event

  Signing of Informed Consent (<=28 Days Prior to Day -1, Check-in) to End of Study (Up to 40 Days for Single-Ascending Dose (SAD) Cohorts 1-3 and 5-6; at Least 59 Days for SAD Cohort 4; Up to 53 Days for Multiple-Ascending Dose (MAD) Cohorts 7-10)

• Percentage of Participants with Adverse Events (AEs)

  An AE is any untoward medical occurrence in a participant administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product, whether or not related to the medicinal (investigational) product.

  Signing of Informed Consent (<=28 Days Prior to Day -1, Check-in) to End of Study (Up to 40 Days for Single-Ascending Dose (SAD) Cohorts 1-3 and 5-6; at Least 59 Days for SAD Cohort 4; Up to 53 Days for Multiple-Ascending Dose (MAD) Cohorts 7-10)

• Percentage of Participants with Clinically Significant Abnormalities in Clinical Laboratory Assessments

  Signing of Informed Consent (<=28 Days Prior to Day -1, Check-in) to End of Study (Up to 40 Days for Single-Ascending Dose (SAD) Cohorts 1-3 and 5-6; at Least 59 Days for SAD Cohort 4; Up to 53 Days for Multiple-Ascending Dose (MAD) Cohorts 7-10)

• Percentage of Participants with Clinically Significant Abnormalities in Vital Signs

  Signing of Informed Consent (<=28 Days Prior to Day -1, Check-in) to End of Study (Up to 40 Days for Single-Ascending Dose (SAD) Cohorts 1-3 and 5-6; at Least 59 Days for SAD Cohort 4; Up to 53 Days for Multiple-Ascending Dose (MAD) Cohorts 7-10)

• Percentage of Participants with Clinically Significant Abnormalities in 12-Lead Electrocardiogram (ECG) Parameters

  Signing of Informed Consent (<=28 Days Prior to Day -1, Check-in) to End of Study (Up to 40 Days for Single-Ascending Dose (SAD) Cohorts 1-3 and 5-6; at Least 59 Days for SAD Cohort 4; Up to 53 Days for Multiple-Ascending Dose (MAD) Cohorts 7-10)

• Percentage of Participants with Clinically Significant Abnormalities in Physical Examinations

  Signing of Informed Consent (<=28 Days Prior to Day -1, Check-in) to End of Study (Up to 40 Days for Single-Ascending Dose (SAD) Cohorts 1-3 and 5-6; at Least 59 Days for SAD Cohort 4; Up to 53 Days for Multiple-Ascending Dose (MAD) Cohorts 7-10)

Secondary Outcomes (12)

• Area Under the Concentration-Time Curve (AUC) from Time Zero to the Time of the Last Measurable Concentration (AUClast)

  Multiple Time-points on Days 1 through 4 for Single-Ascending Dose (SAD) Cohorts; Multiple Time-points on Days 1 through 15 for Multiple-Ascending Dose (MAD) Cohorts

• AUC from Time Zero Extrapolated to Infinity (AUC∞)

  Multiple Time-points on Days 1 through 4 for Single-Ascending Dose (SAD) Cohorts; Multiple Time-points on Days 1 through 15 for Multiple-Ascending Dose (MAD) Cohorts

• AUC Within a Dosing Interval (AUCtau)

  Multiple Time-points on Days 1 through 4 for Single-Ascending Dose (SAD) Cohorts; Multiple Time-points on Days 1 through 15 for Multiple-Ascending Dose (MAD) Cohorts

• Maximum Observed Concentration (Cmax)

  Multiple Time-points on Days 1 through 4 for Single-Ascending Dose (SAD) Cohorts; Multiple Time-points on Days 1 through 15 for Multiple-Ascending Dose (MAD) Cohorts

• Trough Concentration (Ctrough)

  Multiple Time-points on Days 1 through 4 for Single-Ascending Dose (SAD) Cohorts; Multiple Time-points on Days 1 through 15 for Multiple-Ascending Dose (MAD) Cohorts

Study Arms (11)

Cohort 1: BIIB095 5 mg

EXPERIMENTAL

Following an overnight fast from food of at least 8 hours, participants will receive a single dose of either BIIB095 5 mg or placebo orally, followed by a fast of at least 4 hours post dose.

Drug: BIIB095; Drug: Placebo

Cohort 2: BIIB095 25 mg

EXPERIMENTAL

Following an overnight fast from food of at least 8 hours, participants will receive a single dose of either BIIB095 25 mg or placebo orally, followed by a fast of at least 4 hours post dose.

Drug: BIIB095; Drug: Placebo

Cohort 3: BIIB095 100 mg

EXPERIMENTAL

Following an overnight fast from food of at least 8 hours, participants will receive a single dose of either BIIB095 100 mg or placebo orally, followed by a fast of at least 4 hours post dose.

Drug: BIIB095; Drug: Placebo

Cohort 4 (Fasted): BIIB095 200 mg

EXPERIMENTAL

Following an overnight fast from food of at least 8 hours, participants will receive a single dose of either BIIB095 200 mg or placebo orally, followed by a fast of at least 4 hours post dose.

Drug: BIIB095; Drug: Placebo

Cohort 4 (Fed): BIIB095 200 mg

EXPERIMENTAL

After a minimum 2 week washout period, followed by an overnight fast of at least 8 hours, participants will consume a high fat breakfast. Participants will then receive a single dose of either BIIB095 200 mg or placebo orally within 30 minutes after starting the breakfast, followed by a fast from food for at least 4 hours post dose.

Drug: BIIB095; Drug: Placebo

Cohort 5: BIIB095 400 mg

EXPERIMENTAL

Following an overnight fast from food of at least 8 hours, participants will receive a single dose of either BIIB095 400 mg or placebo orally, followed by a fast of at least 4 hours post dose.

Drug: BIIB095; Drug: Placebo

Cohort 6: BIIB095 600 mg

EXPERIMENTAL

Following an overnight fast from food of at least 8 hours, participants will receive a single dose of either BIIB095 600 mg or placebo orally, followed by a fast of at least 4 hours post dose.

Drug: BIIB095; Drug: Placebo

Cohort 7: BIIB095 50 mg BID

EXPERIMENTAL

Participants will receive a single dose of either BIIB095 50 mg or placebo orally BID approximately 12 hours apart from Days 1 to 13, and once in the morning on Day 14. Morning doses will be preceded by an overnight fast from food of at least 8 hours and will be followed by a fast of at least 2 hours post dose. Evening doses will be preceded by a fast from food of at least 2 hours and will be followed by a fast of at least 2 hours post dose.

Drug: BIIB095; Drug: Placebo

Cohort 8: BIIB095 100 mg BID

EXPERIMENTAL

Participants will receive a single dose of either BIIB095 100 mg or placebo orally BID approximately 12 hours apart from Days 1 to 13, and once in the morning on Day 14. Morning doses will be preceded by an overnight fast from food of at least 8 hours and will be followed by a fast of at least 2 hours post dose. Evening doses will be preceded by a fast from food of at least 2 hours and will be followed by a fast of at least 2 hours post dose.

Drug: BIIB095; Drug: Placebo

Cohort 9: BIIB095 200 mg BID

EXPERIMENTAL

Participants will receive a single dose of either BIIB095 200 mg or placebo orally BID approximately 12 hours apart from Days 1 to 13, and once in the morning on Day 14. Morning doses will be preceded by an overnight fast from food of at least 8 hours and will be followed by a fast of at least 2 hours post dose. Evening doses will be preceded by a fast from food of at least 2 hours and will be followed by a fast of at least 2 hours post dose.

Drug: BIIB095; Drug: Placebo

Cohort 10: BIIB095 300 mg BID

EXPERIMENTAL

Participants will receive a single dose of either BIIB095 300 mg or placebo orally BID approximately 12 hours apart from Days 1 to 13, and once in the morning on Day 14. Morning doses will be preceded by an overnight fast from food of at least 8 hours and will be followed by a fast of at least 2 hours post dose. Evening doses will be preceded by a fast from food of at least 2 hours and will be followed by a fast of at least 2 hours post dose.

Drug: BIIB095; Drug: Placebo

Interventions

BIIB095 DRUG

Administered as specified in the treatment arm.

Cohort 10: BIIB095 300 mg BID; Cohort 1: BIIB095 5 mg; Cohort 2: BIIB095 25 mg; Cohort 3: BIIB095 100 mg; Cohort 4 (Fasted): BIIB095 200 mg; Cohort 4 (Fed): BIIB095 200 mg; Cohort 5: BIIB095 400 mg; Cohort 6: BIIB095 600 mg; Cohort 7: BIIB095 50 mg BID; Cohort 8: BIIB095 100 mg BID; Cohort 9: BIIB095 200 mg BID

Placebo DRUG

Administered as specified in the treatment arm.

Cohort 10: BIIB095 300 mg BID; Cohort 1: BIIB095 5 mg; Cohort 2: BIIB095 25 mg; Cohort 3: BIIB095 100 mg; Cohort 4 (Fasted): BIIB095 200 mg; Cohort 4 (Fed): BIIB095 200 mg; Cohort 5: BIIB095 400 mg; Cohort 6: BIIB095 600 mg; Cohort 7: BIIB095 50 mg BID; Cohort 8: BIIB095 100 mg BID; Cohort 9: BIIB095 200 mg BID

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Ability of the subject to understand the purpose and risks of the study and provide signed and dated informed consent and authorization to use confidential health information in accordance with national and local subject privacy regulations.
• Must have a body mass index between 18 and 30 kg/m2, inclusive.
• All women of childbearing potential and all men must practice highly effective contraception during the study and for 5 times the half-life or 3 months, whichever is longer, after their last dose of study treatment. In addition, subjects should not donate sperm or eggs during the study and for at least 3 months after their last dose of study treatment.
• Must be in good health as determined by the Investigator, based on medical history and Screening evaluations.

You may not qualify if:

• History of any clinically significant cardiac, endocrine, gastrointestinal, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, or renal disease, or other major disease, as determined by the Investigator.
• Significant history of fainting or vaso-vagal attacks, as determined by the Investigator.
• Current condition known to affect cardiac conduction, or a personal or familial history of Brugada syndrome.
• Congenital nonhemolytic hyperbilirubinemia (Gilbert's syndrome).
• History or risk of seizures or a history of epilepsy, significant head injury or related neurological disorders (excluding childhood febrile convulsions), as determined by the Investigator.
• Current enrollment in any other drug, biologic, device, or clinical study, or treatment with an investigational drug or approved therapy for investigational use within 30 days (6 months for biologics) prior to Day -1, or 5 half-lives of the agent, whichever is longer.
• Exposure to more than 4 experimental chemical entities within 12 months prior to the first dosing day.
• Breastfeeding, pregnant, or planning to become pregnant during study participation

Sponsors & Collaborators

• Biogen: lead

Study Sites (2)

Research Site

Leeds, LS2 9LH, United Kingdom

Location

Hammersmith Medicines Research

London, NW10 7EW, United Kingdom

Location

MeSH Terms

Conditions

Chronic Pain; Neuralgia

Condition Hierarchy (Ancestors)

Pain; Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms; Peripheral Nervous System Diseases; Neuromuscular Diseases; Nervous System Diseases

Study Officials

• Medical Director

  Biogen

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: February 27, 2018
• First Posted: March 5, 2018
• Study Start: March 29, 2018
• Primary Completion: April 30, 2019
• Study Completion: April 30, 2019
• Last Updated: May 16, 2019

Record last verified: 2019-05

Locations

GB (2)