Study to Evaluate the Efficacy and Safety of BIIB074 in Neuropathic Pain From Lumbosacral Radiculopathy

Biogen502 enrolled

Overview

The primary objective of the study is to evaluate the efficacy of two dose regimens of BIIB074 on neuropathic pain in participants with pain from lumbosacral radiculopathy (PLSR). Secondary objectives are to evaluate the efficacy of 2 dose regimens of BIIB074 on additional neuropathic pain measures and assessments of low back pain, disability, and quality of life; To investigate the safety and tolerability of 2 dose regimens of BIIB074 and To characterize the pharmacokinetics (PK) of BIIB074 in this population.

This study was previously posted by Convergence Pharmaceuticals, Ltd., which has been acquired by Biogen.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

502

Conditions

Lumbosacral Radiculopathy

Interventions

BIIB074DRUG

Administered as specified in the treatment arm

PlaceboDRUG

Matched placebo

Eligibility

Sex: ALLMin age: 18 YearsMax age: 75 Years

Medical Language ↔ Plain English

Key Inclusion Criteria: * Has body weight ≥50 kg for men and ≥45 kg for women * Must have diagnosis of neuropathic PLSR * Has duration of neuropathic (leg) pain of at least 6 months before Screening * Has an intensity of ≥4 and ≤9 on the Numerical Rating Scale based on a paper-based question at Screening and on Day 1 that asks for the average pain intensity of neuropathic (leg) pain due to PLSR over the last week Key Exclusion Criteria: * Has planned surgical intervention for PLSR within the duration of the study. (Subjects with persistent radicular pain after prior surgery are eligible.) * Has a history of peripheral neuropathy (e.g., due to diabetes, alcohol consumption, other causes, or idiopathic) or evidence of peripheral neuropathy upon neurological examination * Has a history or risk of seizures or a history of epilepsy, clinically significant head injury, or related neurological disorders NOTE: Other protocol-defined inclusion/exclusion criteria may apply.

Locations (56)

Outcomes

Primary Outcomes

Change from Baseline to Week 14 in the weekly average of the daily neuropathic pain score on the 11-point Pain Intensity Numerical Rating Scale (PI-NRS)

Participants will be asked every evening to rate their overall neuropathic pain for the last 24-hour period. PI-NRS is an 11-point pain intensity numerical rating scale (PI-NRS), where 0=no pain and 10=pain as bad as you can imagine.

Time frame: Week 14

Secondary Outcomes

50% neuropathic daily pain reduction response

Response is defined as a ≥50% reduction in the weekly average of the daily neuropathic pain score from Baseline (Week 2) to Week 14.

Time frame: At Week 14

30% neuropathic daily pain reduction response

Response is defined as a ≥30% reduction in the weekly average of the daily neuropathic pain score from Baseline to Week 14.

Time frame: At Week 14

Change from Baseline to Week 14 in the weekly average of the daily neuropathic pain score at each visit

Time frame: Week 14

Change from Baseline to Week 14 in weekly average of the daily pain score for low back pain

Participants will be asked every evening to rate their overall low back pain for the last 24-hour period

Time frame: Week 14

Number of Patient Global Impression of Change (PGIC) responders

PGIC is a 7-point, self-report scale depicting a participant's rating of overall improvement. Participants rate their change as "very much improved," "much improved," "minimally improved," "no change," "minimally worse," "much worse," or "very much worse."

Time frame: At Week 14

Data from ClinicalTrials.gov

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Research Site

Klagenfurt, Austria

Research Site

Leuven, Belgium

Research Site

Blagoevgrad, Bulgaria

Research Site

Rousse, Bulgaria

Research Site

Sofia, Bulgaria

Research Site

Sofia, Bulgaria

Research Site

Sofia, Bulgaria

Research Site

Sofia, Bulgaria

Research Site

Veliko Tarnovo, Bulgaria

Research Site

Beroun, Czechia

...and 46 more locations

Change from Baseline to Week 14 on the Oswestry Disability Index

This is a 10-item questionnaire that evaluates how back (or leg) pain affects the ability to manage in everyday life. Each question is rated on a 5 point scale with higher scores indicating higher level of pain.

Change from Baseline to Week 14 in the weekly average of daily sleep score as assessed by the Sleep Numerical Rating Scale (S-NRS)

Participants will be asked every morning to rate on the 11-point S-NRS how leg pain interfered with their sleep quality, where 0=no pain and 10=Pain completely interfered with sleep.

Time frame: Week 14

Change from Baseline to Week 14 in the Brief Pain Inventory (BPI)- Interference index

BPI Interference Index is an 11-point numeric rating scale (0 - no interference to 10 - interferes completely) to assess pain-related interference in 7 areas: general activity, mood, walking ability, normal work, including outside the home and housework, relations with other people, enjoyment of life and sleep.

Time frame: Week 14

Change from Baseline to Week 14 in the BPI-Pain index

BPI- Pain Index for pain intensity is used to assess potential pain quality descriptors that may describe participants' pain on a scale of 0 (no pain) to 10 (pain as bad as you can imagine).

Time frame: Week 14

Change from Baseline to Week 14 on the EuroQoL 5-Dimension 5-Level Questionnaire (EQ-5D-5L) health index

The EQ-5D-3L is a standardized instrument for use as a measure of health outcome. It is a health questionnaire that consists of the EQ-5D descriptive system and the EQ visual analogue scale (EQ VAS). The EQ-5D-3L descriptive system comprises the following 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 3 levels: no problems, some problems, extreme problems.

Time frame: Week 14

Change from Baseline to Week 14 in Short Form 36 Questionnaire (SF-36)

SF-36 is a self-administered, generic health status questionnaire consisting of 36 questions that measure 8 health concepts: physical functioning, role limitations due to physical problems, bodily pain, general health perception, vitality, social functioning, role limitations due to emotional problems and mental health.

Time frame: Week 14

Amount of rescue medication used per day

Time frame: Day 1 to Week 15

Number of participants experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)

Time frame: Up to Week 15

Number of participants with clinically significant vital sign abnormalities

Time frame: Up to Week 15

Number of participants with clinically significant 12-lead electrocardiograms (ECGs) abnormalities

Time frame: Up to Week 15

Number of participants with clinically significant laboratory assessment abnormalities

Time frame: Up to Week 15

Safety and Tolerability as assessed by Columbia-Suicide Severity Rating Scale (C-SSRS)

C-SSRS is a suicidal ideation rating used to evaluate suicidality in children ages 12 and up. It rates an individual's degree of suicidal ideation on a scale, ranging from "wish to be dead" to "active suicidal ideation with specific plan and intent."

Time frame: Up to Week 15

Area under the concentration-time curve over the dosing period (AUCtau) at steady state

Time frame: 30 min prior to dosing up to 8 hours post dose

Maximum concentration (Cmax)

Time frame: 30 min prior to dosing up to 8 hours post dose