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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.

Visão geral do estudo

Status

Ainda não está recrutando

Intervenção / Tratamento

Descrição detalhada

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 estudo

Intervencional

Inscrição (Estimado)

24

Estágio

  • Fase inicial 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

    • Kansas
      • Overland Park, Kansas, Estados Unidos, 66212
        • Dr. Vince Clinical Research
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  1. Is willing and able to provide informed consent and comply with all protocol requirements
  2. Is aged ≥18 years and ≤55 years at time of informed consent
  3. Has a body mass index (BMI) between 18.0 and 32.0 kg/m2 and body weight (BW) not lower than 50 kg
  4. 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)
  5. Has Blood pressure (BP) and Heart rate (HR) within the normal range at the Screening visit after 5 minutes in a seated position:

    1. Systolic BP between 90 and 145 mmHg
    2. Diastolic BP between 60 and 90 mmHg
    3. HR between 60 and 90 beats per minute
  6. Electrocardiogram (ECG) is normal based on 12-lead ECG assessment at Screening:

    1. ECG PR interval between 120 and 200 ms
    2. ECG QRS interval <100 ms
    3. ECG QT interval (corrected) (QTc) with Fridericia formula (QTcF) <450 ms and no history of additional risk factors for Torsades de pointes (TdP)
    4. No sign of any sinus node dysfunction
  7. 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.
  8. 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.
  9. 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).
  10. If female, must have a negative serum or urine pregnancy test at Screening and a negative serum or urine test at Admission (day 1)
  11. 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.
  12. 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:

  1. Any significant acute or chronic medical illness
  2. Any history of cancer within 5 years of enrollment, with the exception of fully resected skin basal cell carcinoma
  3. Any major hospitalization or surgery 3 months prior to study drug administration
  4. 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
  5. Poor venous access assessed at Screening
  6. 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
  7. 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
  8. 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
  9. 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)
  10. Any neurological, renal, cardiac, hepatic, or other medical condition that could interfere with study assessments as determined by and Investigator, or Sponsor
  11. Any significant illness or infection, as determined by an Investigator or Sponsor, within the prior 30 days
  12. Positive urine alcohol or urine drug screen for substance of abuse at Screening
  13. Must not be physically dependent on opioids, as demonstrated by successful completion of the naloxone challenge
  14. Known hypersensitivity to any component of the MCAM drug product, naloxone, or placebo
  15. 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
  16. Positive screen for hepatitis B surface antigen (HBsAg), Hepatitis C (HCV) antibody, or HIV-1 and HIV-2 antibodies
  17. 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)
  18. Is likely, in the opinion of an Investigator, to be non-compliant or uncooperative with study procedures for any reason
  19. If female, are pregnant, nursing, or planning to become pregnant during the study

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Ciência básica
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Dobro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
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.
MCAM will be dosed orally as a 3, 10, or 30 mg suspension in an amber syringe to maintain blinding.
Comparador de Placebo: Single Ascending Group Placebo
Participants randomized to placebo will receive 1% methylcellulose solution on Day 1.
A 1% methylcellulose solution will be dosed orally using an amber syringe to maintain blinding.
Outros nomes:
  • methylcellulose solution

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Single Ascending Dose (SAD): Cmax
Prazo: Baseline to 96 hours
Maximum plasma concentration in the blood after administration
Baseline to 96 hours
SAD: Tmax
Prazo: Baseline to 96 hours
Time to maximum concentration of drug in the blood
Baseline to 96 hours
SAD: T1/2
Prazo: Baseline to 96 hours
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 96 hours
SAD: Area under the curve from 0-24 hours
Prazo: Baseline to 96 hours
Area under the plasma concentration time curve from time 0 to 24 hours
Baseline to 96 hours
SAD: Area under the curve from 0-t
Prazo: Baseline to 96 hours
Area under the plasma concentration time curve from time 0 to the last measurable concentration
Baseline to 96 hours
SAD: Area under the curve from 0-infinity
Prazo: Baseline to 96 hours
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 96 hours

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Part B (Opioid-Experienced Cohort): Cmax
Prazo: Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
Maximum concentration of drug in the blood
Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
Part B (Opioid-Experienced Cohort): Tmax
Prazo: Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
Time to maximum concentration of drug in the blood
Baseline to 24 hours for placebo and baseline to 216 hours for MCAM
Part B (Opioid-Experienced Cohort): T1/2
Prazo: 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
Part B (Opioid-Experienced Cohort): Area under the curve from 0-24 hours
Prazo: 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
Part B (Opioid-Experienced Cohort): Area under the curve from 0-t
Prazo: 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
Part B Opioid-Experienced Cohort: Area under the curve from 0-infinity
Prazo: 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

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Benjamin Sundling, DO, Dr. Vince Clinical Research

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

8 de agosto de 2026

Conclusão Primária (Estimado)

30 de junho de 2027

Conclusão do estudo (Estimado)

31 de dezembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

15 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

15 de maio de 2026

Primeira postagem (Real)

22 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

11 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

8 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • UTHSCSA-MCAM-101
  • U01DA060704 (Concessão/Contrato do NIH dos EUA)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

The results of the study will be used for the purposes of national and international registration, publication, and information for medical and pharmaceutical professionals.

Prazo de Compartilhamento de IPD

At study end, once the data is analyzed and published in a peer review journal

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA
  • CIF

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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