A Study to Assess the Safety, Tolerability, and Pharmacokinetics of BIIB078 in Adults With C9ORF72-Associated Amyotrophic Lateral Sclerosis

• Sponsor: Biogen (Industry)
• Overall Status: Completed
• CT.gov ID: NCT03626012
• Collaborator: (none)
• Enrollment: 106
• Locations: 21
• Arms: 7
• Actual Duration (Months): 38.2
• Patients Per Site: 5
• Patients Per Site Per Month: 0.1

Study Details

Study Description

Brief Summary

The primary objective of this study is to evaluate the safety and tolerability of BIIB078 in adults with C9ORF72-Amyotrophic Lateral Sclerosis (ALS). The secondary objectives of this study are to evaluate the pharmacokinetic profile of BIIB078 and to evaluate the effects of BIIB078 on clinical function. As the first-in-human study, the study enrolls a small number of participants in each cohort. Every participant in a cohort is treated with the same dose or placebo. The study is designed to evaluate and confirm the safety of each dose before enrolling and exposing new participants to a higher dose in the next cohort.

Condition or Disease	Intervention/Treatment	Phase
Amyotrophic Lateral Sclerosis	Drug: BIIB078; Drug: Placebo	Phase 1

Study Design

• Study Type: Interventional
• Actual Enrollment: 106 participants
• Allocation: Randomized
• Intervention Model: Sequential Assignment
• Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
• Primary Purpose: Treatment
• Official Title: A Phase 1 Multiple-Ascending-Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of BIIB078 Administered Intrathecally to Adults With C9ORF72-Associated Amyotrophic Lateral Sclerosis
• Actual Study Start Date: Sep 10, 2018
• Actual Primary Completion Date: Nov 17, 2021
• Actual Study Completion Date: Nov 17, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Cohort 1: BIIB078 First Dosage BIIB078 will be administered as a loading regimen of 3 doses, on Day 1 and two later days, followed by two maintenance doses on two later days.	Drug: BIIB078; Administered as specified in the treatment arm.
Experimental: Cohort 2: BIIB078 Second Dosage BIIB078 will be administered as a loading regimen of 3 doses, on Day 1 and two later days, followed by two maintenance doses on two later days.	Drug: BIIB078; Administered as specified in the treatment arm.
Experimental: Cohort 3: BIIB078 Third Dosage BIIB078 will be administered as a loading regimen of 3 doses, on Day 1 and two later days, followed by two maintenance doses on two later days.	Drug: BIIB078; Administered as specified in the treatment arm.
Experimental: Cohort 4: BIIB078 Fourth Dosage BIIB078 will be administered as a loading regimen of 3 doses, on Day 1 and two later days, followed by five maintenance doses on five later days.	Drug: BIIB078; Administered as specified in the treatment arm.
Experimental: Cohort 5: BIIB078 Fifth Dosage BIIB078 will be administered as a loading regimen of 3 doses, on Day 1 and two later days, followed by five maintenance doses on five later days.	Drug: BIIB078; Administered as specified in the treatment arm.
Experimental: Cohort 6: BIIB078 Sixth Dosage BIIB078 will be administered as a loading regimen of 3 doses, on Day 1 and two later days, followed by five maintenance doses on five later days.	Drug: BIIB078; Administered as specified in the treatment arm.
Placebo Comparator: Cohorts 1-6: Placebo Matching placebo will be administered as a loading regimen of 3 doses, on Day 1 and two later days, followed by two maintenance doses on two later days (Cohorts 1 through 3) and five maintenance doses on five later days (Cohorts 4 through 6).	Drug: Placebo; Administered as specified in the treatment arm.

Outcome Measures

Primary Outcome Measures

1. Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) [Baseline through End of Study (Approximately Day 323)]

   An AE is any untoward medical occurrence in a participant who received study drug without regard to possibility of causal relationship. An SAE is an AE resulting in any of the following outcomes or deemed significant for any other reason: death, places participant at immediate risk of death, requires initial or prolonged inpatient hospitalization, results in persistent or significant disability/incapacity, results in congenital anomaly, is a medically important event.

Secondary Outcome Measures

1. Serum BIIB078 Concentration [Baseline and at multiple time points up to Day 260]

2. Area Under the Concentration-Time Curve (AUC) from Time 0 to Infinity (AUCinf) [Baseline and at multiple time points up to Day 260]

3. AUC from Time 0 to Time of the Last Measurable Concentration (AUClast) [Baseline and at multiple time points up to Day 260]

4. Maximum Observed Concentration (Cmax) [Baseline and at multiple time points up to Day 260]

5. Time to Reach Cmax (Tmax) [Baseline and at multiple time points up to Day 260]

6. Terminal Elimination Half-Life (t 1/2) [Baseline and at multiple time points up to Day 260]

7. Change from Baseline in Amyotrophic Lateral Sclerosis Functional Rating Scale - Revised (ALSFRS-R) Scores [Baseline up to Day 323]

   The ALSFRS-R has been demonstrated to predict survival. The ALSFRS-R measures 4 functional domains, including respiratory, bulbar function, gross motor skills, and fine motor skills. There are a total of 12 questions, each scored from 0 to 4 for a total possible score of 48 [Cedarbaum 1999], with higher scores representing better function.

8. Change from Baseline in Percent of Predicted Slow Vital Capacity (SVC) [Baseline up to Day 260]

9. Change from Baseline in Muscle Strength [Baseline up to Day 260]

   Quantitative muscle strength will be evaluated using hand-held dynamometry (HHD), which tests isometric strength of multiple muscles using standard participant positioning. Approximately 8 muscle groups will be examined (per each side) in both upper and lower extremities.

10. Change from Baseline in Bulbar Strength [Baseline up to Day 260]

    Bulbar strength will be measured by the Iowa Oral Pressure Instrument (IOPI). The IOPI is a commercially available tongue pressure measurement system composed of an air-filled bulb connected to a pressure transducer. The bulb can be placed in different positions in the mouth in order to assess different aspects of tongue weakness.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Key Inclusion Criteria:

• Ability of the participant to understand the purpose and risks of the study, to provide signed and dated informed consent, and to authorize the use of confidential health information in accordance with national and local participant privacy regulations; or, in the event of the participant's physical incapacity to sign, to confirm that understanding and consent orally to a legally authorized representative (LAR) for the express purpose of having said informed consent and authorization signed on his/her behalf.

• All participants of childbearing potential must agree to practice highly effective contraception during the study and be willing and able to continue contraception for 5 months after their last dose of study treatment.

• Must meet the possible, laboratory-supported probable, probable, or definite criteria for diagnosing ALS according to the World Federation of Neurology El Escorial criteria and have documentation of a clinical genetic test demonstrating the presence of a pathogenic mutation in C9ORF72.

• Slow vital capacity (SVC) ≥ 50% of predicted value as adjusted for sex, age, and height (from the sitting position).

• Participants taking concomitant riluzole at study entry must be on a stable dose for ≥ 30 days prior to the first dose of study treatment (Day 1).

• Participants taking concomitant edaravone at study entry must be on a stable dose for ≥ 60 days prior to the first dose of study treatment (Day 1).

• ALS Cognitive Behavioral Screen (ALS-CBS) score ≥ 11 for the cognitive portion; ≥ 33 for the behavioral portion.

• Medically able to undergo the study procedures, and to adhere to the visit schedule at the time of study entry, as determined by the Investigator.

• Screening values of coagulation parameters including platelet count, international normalized ratio (INR), prothrombin time (PT), and activated partial thromboplastin time (APTT) should be within normal ranges.

• Has an informant/caregiver who, in the Investigator's judgment, has frequent and sufficient contact with the participant as to be able to provide accurate information about the participant's cognitive and functional abilities at Screening.

Key Exclusion Criteria:

• History of drug abuse or alcoholism ≤ 6 months of Screening that would limit participation in the study, as determined by the Investigator.

• Tracheostomy.

• Prescreening ALSFRS-R slope less than 0.4 points/month, where prescreening ALSFRS-R slope is defined as follows: (48 - ALSFRS-R score at Screening) / (months from date of symptom onset to date of Screening).

• History of or positive test result at Screening for human immunodeficiency virus. .

• History of, or positive test result at Screening for, hepatitis C virus antibody.

• Treatment with another investigational drug or biological agent within 1 month of Screening or 5 half-lives of study agent, whichever is longer.

• Treatment with an antiplatelet or anticoagulant therapy that cannot safely be interrupted for lumbar puncture (LP) according to local standard of care and/or institutional guidelines, in the opinion of the Investigator or Prescriber.

• Current or anticipated need, in the opinion of the Investigator, of a diaphragm pacing system during the study period.

• Female participants who are pregnant or currently breastfeeding.

NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Research Site	La Jolla	California	United States	92037-0886
2	Research Site	Los Angeles	California	United States	90048
3	Research Site	Palo Alto	California	United States	94303
4	Research Site	Jacksonville	Florida	United States	32224
5	Research Site	Miami	Florida	United States	33136
6	Research Site	Atlanta	Georgia	United States	30322
7	Research Site	Baltimore	Maryland	United States	21287
8	Research Site	Boston	Massachusetts	United States	02114
9	Research Site	Saint Louis	Missouri	United States	63110
10	Research Site	Lincoln	Nebraska	United States	68506-2960
11	Research Site	New York	New York	United States	10032
12	Research Site	Knoxville	Tennessee	United States	37920
13	Research Site	Calgary	Alberta	Canada	T2N 1N4
14	Research Site	Toronto	Ontario	Canada	M4N 3M5
15	Research Site	Montreal	Quebec	Canada	H3A 2B4
16	Research Site	Dublin		Ireland	DUBLIN 8
17	Research Site	Utrecht		Netherlands	3508 GA
18	Research Site	St. Gallen		Switzerland	9007
19	Research Site	London	Greater London	United Kingdom	SE5 9RS
20	Research Site	Sheffield	South Yorkshire	United Kingdom	S10 2HQ
21	Research Site	London		United Kingdom	NW1 2PG

Sponsors and Collaborators

• Biogen

Investigators

• Study Director: Medical Director, Biogen

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Biogen
• ClinicalTrials.gov Identifier: NCT03626012
• Other Study ID Numbers: 245AS101; 2017-000294-36
• First Posted: Aug 10, 2018
• Last Update Posted: Jan 14, 2022
• Last Verified: Jan 1, 2022

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Motor Neuron Disease; Amyotrophic Lateral Sclerosis; Sclerosis

Study Results

No Results Posted as of Jan 14, 2022