- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07602335
Safety, Tolerability, and Pharmacokinetics of MCAM in Healthy Adult Participants
A Phase 1, First-In-Human, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single Ascending Doses of MCAM in Randomized Healthy Adult Participants (Double-Blind)
The goal of this clinical trial is to test the safety and to see if there are any side effects of the investigational drug, MCAM. The main aim is to measure blood levels of the study drug after oral administration.
Researchers will compare the active study drug to a placebo to test for any differences between the two groups.
Participants will be screened for up to 28 days before starting study treatment. Following the screening visit, participants will be admitted to a clinic for 4 days for treatment with either the study drug or placebo. They will attend a follow-up visit on Days 5 and 7 and participate in a follow-up phone call on Day 8. Three different doses will be tested to find the highest safe dose.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
A Single ascending dose (SAD) will be administered to evaluate safety, tolerability and pharmacokinetics (PK) of MCAM.
MCAM will be dosed orally to healthy adult participants at one of 3 dose levels: 3, 10, or 30 mg or a matching placebo.
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase temprana 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Charles France, PhD
- Número de teléfono: 210 567 6969
- Correo electrónico: france@uthscsa.edu
Copia de seguridad de contactos de estudio
- Nombre: Julia Taylor, PhD
- Número de teléfono: 210 567 0105
- Correo electrónico: taylorj4@uthscsa.edu
Ubicaciones de estudio
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Kansas
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Overland Park, Kansas, Estados Unidos, 66212
- Dr. Vince Clinical Research
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Contacto:
- Benjamin Sundling, DO
- Número de teléfono: 913-333-3000
- Correo electrónico: bsundling@drvince.com
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Is willing and able to provide informed consent and comply with all protocol requirements
- Is aged ≥18 years and ≤55 years at time of informed consent
- Has a body mass index (BMI) between 18.0 and 32.0 kg/m2 and body weight (BW) not lower than 50 kg
- Participant is a nonsmoker (for at least 3 months prior to Screening) and does not use tobacco-containing products (including but not limited to cigarettes, pipes, cigars, chewing tobacco, or nicotine patch or gum)
Has Blood pressure (BP) and Heart rate (HR) within the normal range at the Screening visit after 5 minutes in a seated position:
- Systolic BP between 90 and 145 mmHg
- Diastolic BP between 60 and 90 mmHg
- HR between 60 and 90 beats per minute
Electrocardiogram (ECG) is normal based on 12-lead ECG assessment at Screening:
- ECG PR interval between 120 and 200 ms
- ECG QRS interval <100 ms
- ECG QT interval (corrected) (QTc) with Fridericia formula (QTcF) <450 ms and no history of additional risk factors for Torsades de pointes (TdP)
- No sign of any sinus node dysfunction
- Has clinical laboratory parameters (hematology [including coagulation], clinical chemistry, and urinalysis) within normal ranges. Individual values out of the normal range may be acceptable if judged clinically insignificant by an Investigator.
- Has not been dosed in an interventional clinical drug trial within 30 days prior to screening or within 5 half-lives of the last dose of study drug, whichever is longer.
- If female, participants who are not of childbearing potential should be surgically sterile (e.g., have undergone hysterectomy, bilateral oophorectomy, bilateral salpingectomy, or tubal ligation/occlusion) or in a post-menopausal state (at least one year without menses). Female participants of childbearing potential will use a highly effective (i.e., failure rate of <1%) method of contraception throughout the study and for at least five half-lives following MCAM dosing. Methods of contraception that are considered to be highly effective with a failure rate of <1% that are appropriate for this study include the following: a) intrauterine device (IUD)/intrauterine system (IUS); b) implantable rod; c) bilateral tubal occlusion; d) complete abstinence from sexual intercourse; and e) infertile male partner (e.g., vasectomized [with documented evidence of azoospermia], permanently sterile following bilateral orchidectomy, or any other documented cause of infertility).
- If female, must have a negative serum or urine pregnancy test at Screening and a negative serum or urine test at Admission (day 1)
- Male participants who report surgical sterilization will be required to confirm sterility by post-vasectomy semen analysis (PVSA). Participants in whom PVSA confirmation cannot be obtained will be required to use a double-barrier method (e.g., condom with spermicide), same as for the rest of the male participants, or agree to remain abstinent from heterosexual intercourse at the time of Screening, during the study, and for at least five half-lives following MCAM dosing.
- If male, participants must agree not to donate sperm for the duration of the study and for 90 days after the last dose of study drug.
Exclusion Criteria:
- Any significant acute or chronic medical illness
- Any history of cancer within 5 years of enrollment, with the exception of fully resected skin basal cell carcinoma
- Any major hospitalization or surgery 3 months prior to study drug administration
- Has donated or experienced a blood loss of 500 mL or more within 56 days prior to Screening or has donated plasma within 7 days prior to Screening
- Poor venous access assessed at Screening
- Has ever participated or plans to participate in a substance or alcohol rehabilitation program to treat their substance or alcohol dependence. If participation in a rehabilitation program was court-mandated as part of a plea agreement, entry may be permissible at an Investigator's discretion
- Any history of substance use disorder) as defined in the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5; e.g. a score of ≥2, within a 12-month period) or recent use of an opioid-containing product (e.g., codeine) within 6 months prior to study drug administration
- History of, or currently diagnosed with, any clinically significant psychiatric disorder (based on the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition [DSM-5] and Mini International Neuropsychiatric Interview [MINI] criteria), which in the opinion of an Investigator could interfere with study participation or study data collection
- History of any suicidal ideation within the past 6 months or a lifetime history of suicidal behavior, as assessed by the Columbia-Suicide Severity Rating Scale (C-SSRS)
- Any neurological, renal, cardiac, hepatic, or other medical condition that could interfere with study assessments as determined by and Investigator, or Sponsor
- Any significant illness or infection, as determined by an Investigator or Sponsor, within the prior 30 days
- Positive urine alcohol or urine drug screen for substance of abuse at Screening
- Must not be physically dependent on opioids, as demonstrated by successful completion of the naloxone challenge
- Known hypersensitivity to any component of the MCAM drug product, naloxone, or placebo
- Use of any prescription or over-the-counter medications (such as antacids, vitamins, minerals, dietary/herbal preparations, St. John's Wort, and nutritional supplements) within 14 days prior to Screening or 5 half-lives prior to the study
- Positive screen for hepatitis B surface antigen (HBsAg), Hepatitis C (HCV) antibody, or HIV-1 and HIV-2 antibodies
- Have a procedure planned that would require the use of opioids for pain management within at least 2 weeks after the conclusion of the study (participants may be resistant to opioids for two weeks or longer after study participation)
- Is likely, in the opinion of an Investigator, to be non-compliant or uncooperative with study procedures for any reason
- If female, are pregnant, nursing, or planning to become pregnant during the study
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Ciencia básica
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Doble
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Single Ascending Group (SAD) MCAM
MCAM will be dosed orally using 3 dose levels: 3, 10 and 30 mg free base on Day 1.
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MCAM will be dosed orally as a 3, 10, or 30 mg suspension in an amber syringe to maintain blinding.
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Comparador de placebos: Single Ascending Group Placebo
Participants randomized to placebo will receive 1% methylcellulose solution on Day 1.
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A 1% methylcellulose solution will be dosed orally using an amber syringe to maintain blinding.
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Single Ascending Dose (SAD): Cmax
Periodo de tiempo: Baseline to 96 hours
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Maximum plasma concentration in the blood after administration
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Baseline to 96 hours
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SAD: Tmax
Periodo de tiempo: Baseline to 96 hours
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Time to maximum concentration of drug in the blood
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Baseline to 96 hours
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SAD: T1/2
Periodo de tiempo: Baseline to 96 hours
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Known as the "plasma half-life," this is the time required for the concentration of a substance (like a drug) in blood plasma to decrease by half its initial value.
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Baseline to 96 hours
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SAD: Area under the curve from 0-24 hours
Periodo de tiempo: Baseline to 96 hours
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Area under the plasma concentration time curve from time 0 to 24 hours
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Baseline to 96 hours
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SAD: Area under the curve from 0-t
Periodo de tiempo: Baseline to 96 hours
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Area under the plasma concentration time curve from time 0 to the last measurable concentration
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Baseline to 96 hours
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SAD: Area under the curve from 0-infinity
Periodo de tiempo: Baseline to 96 hours
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Area Under the Curve from time zero to infinity (AUC 0-infinity) is a fundamental pharmacokinetic parameter representing the total drug exposure over time, from administration until the drug is completely eliminated.
It measures the entire extent of absorption, distribution, metabolism, and excretion.
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Baseline to 96 hours
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Part B (Opioid-Experienced Cohort): Cmax
Periodo de tiempo: Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
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Maximum concentration of drug in the blood
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Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
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Part B (Opioid-Experienced Cohort): Tmax
Periodo de tiempo: Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
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Time to maximum concentration of drug in the blood
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Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
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Part B (Opioid-Experienced Cohort): T1/2
Periodo de tiempo: Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
|
Known as the "plasma half-life," this is the time required for the concentration of a substance (like a drug) in blood plasma to decrease by half its initial value.
|
Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
|
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Part B (Opioid-Experienced Cohort): Area under the curve from 0-24 hours
Periodo de tiempo: Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
|
Area under the plasma concentration time curve from time 0 to the last measurable concentration
|
Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
|
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Part B (Opioid-Experienced Cohort): Area under the curve from 0-t
Periodo de tiempo: Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
|
Area under the plasma concentration time curve from time 0 to the last measurable concentration
|
Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
|
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Part B Opioid-Experienced Cohort: Area under the curve from 0-infinity
Periodo de tiempo: Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
|
Area Under the Curve from time zero to infinity (AUC 0-infinity) is a fundamental pharmacokinetic parameter representing the total drug exposure over time, from administration until the drug is completely eliminated.
It measures the entire extent of absorption, distribution, metabolism, and excretion.
|
Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
|
Colaboradores e Investigadores
Colaboradores
Investigadores
- Investigador principal: Benjamin Sundling, DO, Dr. Vince Clinical Research
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
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
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- UTHSCSA-MCAM-101
- U01DA060704 (Subvención/contrato del NIH de EE. UU.)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Marco de tiempo para compartir IPD
Tipo de información de apoyo para compartir IPD
- PROTOCOLO DE ESTUDIO
- SAVIA
- CIF
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.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .