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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.

Studieoversikt

Status

Har ikke rekruttert ennå

Intervensjon / Behandling

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Antatt)

24

Fase

  • Tidlig fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

    • Kansas
      • Overland Park, Kansas, Forente stater, 66212
        • Dr. Vince Clinical Research
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Ja

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Grunnvitenskap
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
Placebo komparator: 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.
Andre navn:
  • methylcellulose solution

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Single Ascending Dose (SAD): Cmax
Tidsramme: Baseline to 96 hours
Maximum plasma concentration in the blood after administration
Baseline to 96 hours
SAD: Tmax
Tidsramme: Baseline to 96 hours
Time to maximum concentration of drug in the blood
Baseline to 96 hours
SAD: T1/2
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Part B (Opioid-Experienced Cohort): Cmax
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Benjamin Sundling, DO, Dr. Vince Clinical Research

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

8. august 2026

Primær fullføring (Antatt)

30. juni 2027

Studiet fullført (Antatt)

31. desember 2027

Datoer for studieregistrering

Først innsendt

15. mai 2026

Først innsendt som oppfylte QC-kriteriene

15. mai 2026

Først lagt ut (Faktiske)

22. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

11. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

8. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • UTHSCSA-MCAM-101
  • U01DA060704 (U.S. NIH-stipend/kontrakt)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-planbeskrivelse

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

IPD-delingstidsramme

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

IPD-deling Støtteinformasjonstype

  • STUDY_PROTOCOL
  • SEVJE
  • ICF

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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