LMN-201 para la prevención de la recurrencia de la infección por C. difficile
Un estudio de fase 2, aleatorizado, doble ciego, controlado con placebo de LMN-201 para la prevención de la recurrencia de la infección por C. difficile
This is a multisite study to evaluate the safety, tolerability, and efficacy of LMN-201 in participants recently diagnosed with CDI who are scheduled to receive or are receiving SOC antibiotic therapy against C. difficile.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
- Fase 3
Contactos y Ubicaciones
Ubicaciones de estudio
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California
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Escondido, California, Estados Unidos, 90027
- Kaiser Permanente
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Connecticut
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Hamden, Connecticut, Estados Unidos, 06518
- Gastroenterology Center of Connecticut
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Florida
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Tampa, Florida, Estados Unidos, 33606
- University of South Florida
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Illinois
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Burr Ridge, Illinois, Estados Unidos, 60527
- Metro Infectious Disease Consultants, LLC
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Kentucky
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Lexington, Kentucky, Estados Unidos, 40503
- Baptist Health Research
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Michigan
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Detroit, Michigan, Estados Unidos, 48202
- Henry Ford Health System
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Minnesota
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Minneapolis, Minnesota, Estados Unidos, 55455
- University of Minnesota
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Rochester, Minnesota, Estados Unidos, 55905
- Mayo Clinic - Rochester
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New York
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New York, New York, Estados Unidos, 10021
- Weill Cornell Medicine
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North Carolina
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Mount Airy, North Carolina, Estados Unidos, 27030
- IMA Clinical Research
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Texas
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Houston, Texas, Estados Unidos, 77030
- MD Anderson Cancer Center
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Virginia
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Annandale, Virginia, Estados Unidos, 22003
- Clinical Alliance for Infectious Diseases - Infectious Diseases, LLC
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Charlottesville, Virginia, Estados Unidos, 22903
- University of Virginia School of Medicine
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Springfield, Virginia, Estados Unidos, 22015
- Kaiser Permanente-Mid Atlantic
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Wisconsin
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Madison, Wisconsin, Estados Unidos, 53792
- UW Health University Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Male or female, aged 18 or older.
- Diagnosis of CDI defined as a new or recent history of 3 or more bowel movements per day with a loose or watery consistency (Bristol Stool Scale 5, 6, or 7); a positive stool C. difficile toxin B immunoassay (stool collected no more than 7 days before first dose of LMN-201/placebo), and no other likely explanation for diarrhea. NOTE: Diarrhea is not required to be present on the day of enrollment.
- Provision of signed and dated informed consent form.
- Scheduled to receive or planning to receive a ≤28-day course of SOC antibiotic therapy for CDI. Participant must have been diagnosed with CDI for 7 or fewer days at time of initial study drug administration. SOC antibiotic therapy is defined as the receipt of oral fidaxomicin or oral metronidazole or oral vancomycin (see Section 8.2.6)
- May be on systemic antibiotics for an infection unrelated to the gastrointestinal tract.
- Ability to take oral medication and willingness to adhere to the study medication regimen.
- Stated willingness and ability to comply with all study procedures and availability for the duration of the study and investigator believes individual will complete the study.
- Access to a mobile smartphone.
- For females of reproductive potential: use of highly effective contraception for at least 4 weeks prior to screening and agreement to use such a method during study participation and for an additional 4 weeks after the end of study drug administration.
- For males of reproductive potential: agreement to use condoms or other methods to ensure effective contraception with partner during study participation and for an additional 4 weeks after the end of study drug administration.
Exclusion Criteria:
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Fulminant C. difficile colitis.
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Admitted or expect to be admitted to an intensive care unit.
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Underlying gastrointestinal disorder characterized by diarrhea including but not limited to chronic ulcerative colitis, Crohn's disease, celiac sprue, short bowel syndrome, dumping syndrome following gastrectomy, pancreatic insufficiency, enteric parasitic infection, viral enteritis, bacterial enteritis (salmonella, shigella, ETEC, etc.).
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Neutropenia (absolute neutrophil count of < 1000 per microliter for any reason).
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Current or previous treatment in past 3 months with any therapy likely to influence the outcome of this study, including but not limited to the following:
- Bezlotoxumab (Zinplava, Merck & Co.), or another antibody against C. difficile toxin(s)
- C. difficile vaccine
- SER-109 (Seres Therapeutics)
- CP101 (Finch Therapeutics)
- VE303 (Vedanta Therapeutics)
- Fecal microbiota transplant
- Current therapy with oral exchange resins
- Protracted exposure to mu-agonist opioids and/or anticholinergic medication prescribed for diarrheal symptoms (unable to stop mu-agonist opioid treatment unless on a stable dose as of onset of diarrhea and no increase in dose planned for the duration of the study.)
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Treatment with SOC antibiotic therapy is planned for longer than a 28-day period.
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Pregnancy, anticipated pregnancy, or breastfeeding.
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Inability or unwillingness to swallow numerous, relatively large capsules containing study drug or placebo because of a swallowing disorder or dysphagia.
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Inability to pass swallowed capsules into the distal small intestine because of gastroparesis, repetitive vomiting, or anatomic narrowing in the esophagus, stomach, or small intestine.
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Psychiatric illness that would affect compliance with medications, study capsules, or follow-up.
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Status as an inmate, residential mental health program, or residential substance abuse program.
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Terminal illness with limited life expectancy of less than 24 weeks.
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Poor concurrent medical risks with clinically significant co-morbid disease such that, in the opinion of the investigator, the patient should not be enrolled.
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Any other condition that, in the opinion of the investigator, would jeopardize the safety or rights of the individual, would make it unlikely for the individual to complete the study, or would confound the results of the study.
- Note: Use of probiotics and other food supplements (e.g., yogurt, kefir, kimchi, etc.) are not exclusionary.
- Note: Assuming participants meet all of the inclusion criteria and none of the exclusion criteria, participants with underlying malignancy with a good life expectancy in the study are not excluded.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Cuadruplicar
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Comparador de placebos: Placebo
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Doses of placebo will be delivered as identical-appearing cornstarch with coloring in size 00, white, opaque, capsules. |
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Experimental: Cohorte centinela
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LMN-201 consists of orally delivered whole, dried, non-viable biomass of spirulina (Arthrospira platensis) grown from 4 separate strains, each of which has been engineered to express one of the following therapeutic proteins:
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Comparador activo: LMN-201
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LMN-201 consists of orally delivered whole, dried, non-viable biomass of spirulina (Arthrospira platensis) grown from 4 separate strains, each of which has been engineered to express one of the following therapeutic proteins:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Proportion of participants who achieve global cure
Periodo de tiempo: Up to 16 weeks after initiation of therapy
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Proportion of total participants with both successful initial CDI treatment and no CDI recurrence during the Prevention and Observation Phases (by treatment assignment). |
Up to 16 weeks after initiation of therapy
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- CDI02
- CDMRP-PR221885 (Otro número de subvención/financiamiento: CDMRP)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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