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Phase 2 N=51 Randomized Double-blind Treatment

Treatment Combining Riluzole and IFB-088 in Bulbar Amyotrophic Lateral Sclerosis (TRIALS Protocol)

Amyotrophic Lateral Sclerosis · ALS

Enrolled (actual)
51
Serious AEs
23.5%
Results posted
Oct 2025
Primary outcome: Primary: Safety Assessment of IFB-088 50 mg/Day in Patients With Bulbar-onset ALS. Number of Participants With Treatment-Emergent Adverse Events [Safety and Tolerability] — 10; 25; 4; 13 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
IFB-088 50mg/day (Drug); Placebo (Drug); Riluzole 100mg/day (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
InFlectis BioScience
Primary completion
Nov 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Safety Assessment of IFB-088 50 mg/Day in Patients With Bulbar-onset ALS. Number of Participants With Treatment-Emergent Adverse Events [Safety and Tolerability]
10; 25; 4; 13; 4; 8
SECONDARY
Efficacy With Scale : ALSFRS-R (ALS Functional Rating Scale Revised)
43.9; 42.2; 39.5; 36.0; 34.7; 36.1 0.923
SECONDARY
Efficacy With Scale : ALS_MITOS (ALS Milano-Torino Staging)
0; 0.1; 0.1; 0.4; 0.6; 0.3 0.398
SECONDARY
Efficacy With Scale : King's College Scale (ALS Staging Form)
1.6; 2.1; 2.1; 2.7; 2.8; 3.0 0.835
SECONDARY
Efficacy Based on Assessment of Respiratory Function (Slow Vital Capacity [SVC])
88.5; 84.7; 74.6; 72.9; 67.9; 69.8 0.481
SECONDARY
Efficacy Based on Assessment of Respiratory Function (Arterial Blood Gases [ABG]), PaCO2)
37.8; 38.5; 38.0; 39.5; 38.7; 38.0
SECONDARY
Efficacy Based on Assessment of Body Composition (Exploratory)
SECONDARY
Pharmacokinetic Parameters (Area Under Curve [AUC])
63; 0; 69; 0
SECONDARY
Pharmacokinetic Parameters (Cmax)
12; 0; 12; 0
SECONDARY
Pharmacokinetic Parameters (Tmax)
1.0; 0; 1.0; 0
SECONDARY
Pharmacokinetic Parameters (t1/2)
4.62; 0; 7.9; 0
SECONDARY
Pharmacokinetic Parameters (Clearance)
580; 0
SECONDARY
Pharmacokinetic Parameters (Vd)
3722; 0
SECONDARY
Biomarkers (TDP-43)
SECONDARY
Biomarkers (Neurofilament Light Chain)
86.57; 65.29; 92.91; 76.19 0.609
SECONDARY
Biomarkers (Inflammation Biomarkers)
704.26; 580.31; 711.31; 572.30; 704.90; 580.13
SECONDARY
Biomarkers (3-Nitrotyrosine)
SECONDARY
Quality of Life With ALSAQ-40 (ALS Assessment Questionnaire)
40.7; 39.5; 67.1; 61.4
SECONDARY
Efficacy Based on Assessment of Respiratory Function (Arterial Blood Gases [ABG]), PO2 (mmHg)
88.8; 97.5; 97.4; 89.1; 91.6; 93.3
SECONDARY
Efficacy Based on Assessment of Respiratory Function (Arterial Blood Gases [ABG]), HCO3 (mEq/L)
24.7; 24.8; 24.8; 24.8; 25.5; 24.6
SECONDARY
Efficacy Based on Assessment of Respiratory Function (Arterial Blood Gases [ABG]), Oxygen Saturation (%)
96; 96.9; 95.2; 96.3; 96.7; 96.6

Summary

Prospective, international, randomised, double-blind, placebo controlled, multicentre, parallel group study. Patients will be randomised in a 2:1 allocation ratio to receive either IFB-088 + riluzole 100 mg or placebo + riluzole 100 mg. This clinical trial is an exploratory study, designed to show a signal of efficacy of IFB-088 through ALSFRS-R, MITOS and King's College. Respiratory function will be followed through SVC. Biomarkers and quality of life will also be evaluated throughout the study. Patients will be treated over a 6-month period. After a screening/consent visit, patients will undergo clinic visits at randomisation (V0), at 2 weeks (V1), and at months 1 (V2), 3 (V3) and 6 (V4). One week after V0, the patient will undergo urine analysis (dipstick)and blood sampling for measurement of creatinine , as well as blood sampling for measurement of creatinine and calculation of eGFR at months 2, 4 and 5. At the V2 visit, in addition to other assessments, patients will undergo blood sampling for PK measurements and urine sampling for crystalluria examination. Blood and urine chemistry, as well as physical examination and vital signs assessment to assess safety will be performed at each visit for safety purpose and crystalluria examination will be repeated at the follow-up visit, performed one month ± one week after V4.

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of probable or definite ALS according to the revised El Escorial criteria [29], with bulbar onset of disease, familial or sporadic form,
  • Onset of symptoms ≤ 18 months prior to screening, as reported by the patient,
  • Adult males or females, aged at least 18 years old,
  • SVC > 60% of predicted value for age and sex,
  • ALSFRS-R score ≥ 36,
  • Treatment with riluzole 100 mg/day, at stable dose since at least one month and well tolerated,
  • Male or female patient of childbearing potential10 who agrees to use highly effective mechanical contraception methods (sexual abstinence, intrauterine device, bilateral tubal occlusion, vasectomised partner) throughout the study, and for 3 months after the end of the treatment,
  • Patient who read, understood and signed the ICF,
  • Patient who is willing to adhere to the study visit schedule and is capable to understand and comply with protocol requirements.

Exclusion Criteria

  • Known other significant neurological disease(s),
  • Serious illness(es) or medical condition(s) (e.g. unstable cardiac disease, cancer, hematologic disease, hepatitis or liver failure, renal failure) that is not stabilised or that could require hospitalisation and may jeopardise the participation in the study,
  • Abnormal renal function at screening defined as estimated glomerular filtration rate (eGFR) 1.5 ULN, and/or AST and/or ALT >3 ULN,
  • Neutropenia (ANC 10 cigarettes per day (e-cigarettes and nicotine patches are permitted),
  • Known hypersensitivity to any of the ingredients or excipients of the IMPs,
  • Pregnant, lactating women,
  • Patient who participated in another trial of investigational drug(s) within 30 days prior to randomisation, or 5 half-lives of the previous investigational product, whichever is longer,
  • Patient who has forfeited their freedom by administrative or legal award, or who is under guardianship or under limited judicial protection.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05508074). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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