NCT05508074Befejeződött2. fázis
Treatment Combining Riluzole and IFB-088 in Bulbar Amyotrophic Lateral Sclerosis (TRIALS Protocol)
A Double-blind, Placebo-controlled, Exploratory Randomised Clinical Trial to Assess the Safety and Efficacy of IFB-088 Plus Riluzole 100 mg vs Placebo Plus Riluzole 100 mg in Patients With Bulbar-onset Amyotrophic Lateral Sclerosis.
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2025. okt. 10.
Rövid összefoglaló (regiszter, angolul)
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.
- Állapot (regiszter)
- Befejeződött
- Fázis (regiszter)
- 2. fázis
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 51 (tényleges)
- Első benyújtás
- 2022. júl. 27.
- Kezdés
- 2022. dec. 2.
- Elsődleges befejezés
- 2024. nov. 14.
- Fő szponzor
- InFlectis BioScience
- Betegségek
- Amiotrófiás laterálszklerózis (ALS)
- NCT-szám
- NCT05508074
- EudraCT-szám
- 2021-003875-32
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó · 2. fázis
- Bevont résztvevők: 51
- 2022. dec. 2. és az elsődleges befejezés (2024. nov. 14.) között
- 9 helyszín, 2 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.
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Korábbi kezelés
- Patient using unauthorised concomitant treatments, namely moderate or strong inhibitors or inducers of CYP1A2, strong inhibitors or inducers of CYP2D6 or 2C19 and strong inhibitors of OCT2, as listed in Section 6.2. Combined oral contraceptives containing ethinylestradiol are forbidden concomitant medications,
- 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,
Más betegség
- 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,
- Non progressive or very rapidly progressing ALS (ALSFRS-R decline from disease onset to randomisation ≤ 0.1 / month or ≥ 1.2 / month)11,
- Dementia or other severe active psychiatric illness, including suicidal ideation assessed using the Columbia-Suicide Severity Rating Scale (C-SSRS),
- Patient with a significant pulmonary disorder not attributed to ALS or who require treatments that might complicate the evaluation of the effect of ALS on respiratory function,
- Known hypersensitivity to any of the ingredients or excipients of the IMPs,
Laborértékek
- Abnormal renal function at screening defined as estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73m2,
- Abnormal liver function at screening defined as total bilirubin levels >1.5 ULN, and/or AST and/or ALT >3 ULN,
- Neutropenia (ANC <1.5 x 109/L) at screening,
Egyéb
- Other causes of neuromuscular weakness,
- Non-invasive ventilation,
- Tracheotomy,
- Weight loss ≥ 10% compared to weight at symptoms onset as declared by the patient or BMI <18 kg/m2 at screening,
- Patient treated by edaravone for ALS,
- Smoker of > 10 cigarettes per day (e-cigarettes and nicotine patches are permitted),
- Pregnant, lactating women,
- Patient who has forfeited their freedom by administrative or legal award, or who is under guardianship or under limited judicial protection.
Kiket keres a vizsgálat
- 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.
Életkor a regiszterben: 18 év – - · Nem: nők és férfiak · Egészséges önkénteseket nem fogad
Helyszínek (9)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| Hôpital Neurologique Pierre Wertheimer | Bron | Franciaország | Ismeretlen állapot |
| APHM Hôpital La Timone Adultes SCE Maladies Neuromusculaires / SLA | Marseille | Franciaország | Ismeretlen állapot |
| CHU de Nantes - Hôpital Laennec | Nantes | Franciaország | Ismeretlen állapot |
| CHU de Toulouse - Hôpital Pierre-Paul Riquet | Toulouse | Franciaország | Ismeretlen állapot |
| CHU Bretonneau | Tours | Franciaország | Ismeretlen állapot |
| Ospedale Civile Sant'Agostino - Estense | Baggiovara | Olaszország | Ismeretlen állapot |
| Centro Clinico NeMO per le Malattie Neuromuscolari | Gussago | Olaszország | Ismeretlen állapot |
| IRCSS Istituto Neurologico Carlo Besta | Milan | Olaszország | Ismeretlen állapot |
| Sant'Andrea Hospital Unit of Neuromuscular Disorders | Roma | Olaszország | Ismeretlen állapot |
Ez az oldal tájékoztatás, nem orvosi tanács. Bármely vizsgálatról az orvosoddal beszélj.