Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Studie av GS-4571 hos friske deltakere, ikke-diabetiske overvektige deltakere og ikke-obese deltakere med type 2 diabetes mellitus (T2DM)

5. oktober 2026 oppdatert av: Gilead Sciences

En fase 1-studie for å evaluere farmakokinetikken, sikkerheten og tolerabiliteten av enkelt stigende orale doser av GS-4571 hos friske deltakere, flere stigende orale doser av GS-4571 hos ikke-diabetiske overvektige deltakere og ikke-obese deltakere med type 2-diabetes mellitus (T2DM), og for å evaluere effekten av mat og et syrereduserende middel på farmakokinetikken til GS-4571

The goal of this clinical study is to learn more about the study drug, GS-4571, and how safe it is in 3 groups, i) Healthy participants, ii) Healthy non-diabetic obese participants, and iii) Non-obese participants with Type 2 Diabetes Mellitus (T2DM).

The primary objectives of this study are:

  • To characterize the pharmacokinetics (PK) of GS-4571 following single and multiple ascending oral doses of GS-4571.
  • To evaluate the effect of concomitant food intake and (if conducted) a representative acid-reducing agent (proton pump inhibitor (PPI), omeprazole) on the PK of GS-4571.
  • To evaluate the safety and tolerability of single and multiple ascending oral doses of GS-4571.

Studieoversikt

Status

Rekruttering

Forhold

Intervensjon / Behandling

Studietype

Intervensjonell

Registrering (Antatt)

134

Fase

  • Fase 1

Kontakter og plasseringer

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

Studiekontakt

Studiesteder

    • Florida
      • Miami, Florida, Forente stater, 33143
        • Rekruttering
        • Qps-Mra, Llc.
    • Texas
      • San Antonio, Texas, Forente stater, 78232
        • Rekruttering
        • ICON Early Phase Services, LLC
    • Utah
      • Salt Lake City, Utah, Forente stater, 84124
        • Rekruttering
        • ICON

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

18 år til 65 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Key Inclusion Criteria:

  • Age 18 through 55 years, for Parts A, B, and C, and 18 through 65 years, for Part D.
  • Individuals must be glucagon-like peptide-1 receptor agonist (GLP-1RA) naïve OR last dose was at least 6 months prior to screening.
  • Part A (SAD) and Part B (Food/PPI Effect): eligible individuals in Cohorts 1-4, (optional cohort 5) and 6 will include healthy individuals with BMI of ≥ 19 and < 30 kg/m^2, and no significant medical history.

Individuals will also be in good general health as determined by the investigator at the screening evaluation performed no more than 28 days prior to the scheduled first dose.

  • Part C (MAD in nondiabetic obese individuals): Eligible individuals in Cohorts 7-9 and (optional cohort 10) will be individuals with obesity with BMI ≥ 30 kg/m^2 and < 45 kg/m^2 with a total body weight > 50 kg, and nondiabetic (HbA1c < 6.5%). Eligible individuals will also be individuals with stable body weight (< 5% change) for 90 days prior to screening visit based on individual report.
  • Part D (multiple doses in non-obese T2DM): eligible individuals in Cohort 11 will be individuals with T2DM HbA1c ≥ 7.0% and ≤ 10.5% with BMI of ≥ 19 and < 30 kg/m^2 and treated with diet and/or exercise, and/or metformin monotherapy.

Key Exclusion Criteria:

  • Have any serious or active medical or psychiatric illness (including depression) that, in the opinion of the investigator, would interfere with individual treatment, assessment, or compliance with the protocol. This would include acute pancreatitis, or history of pancreatitis, acute gallbladder disease, and renal, cardiac, hematological, hepatic, pulmonary (including chronic asthma), endocrine (including diabetes [with the exception of T2DM for individuals included in Part D only]), central nervous, gastrointestinal (including an ulcer), vascular, metabolic (thyroid disorders, adrenal disease), immunodeficiency disorders, active infection, or malignancy that are clinically significant or requiring treatment.
  • Current symptoms of diabetic retinopathy or examination indicating diabetic retinopathy within one year of screening.
  • Any electrolyte disturbances identified at screening considered to be clinically significant in the opinion of the investigator (eg, hypokalemia, hypocalcemia, or hypomagnesemia).
  • Any condition that could lead to electrolyte disturbances (eg, eating disorder) in the opinion of the investigator.
  • History of syncope, palpitations, or unexplained dizziness.
  • Active, or history of, significant cardiac disease or conduction abnormality
  • History of implanted defibrillator or pacemaker.
  • Have been treated with the following within 6 months prior to screening or is expected to receive these agents during the study: GLP-1RAs, systemic steroids, immunosuppressant therapies, or chemotherapeutic agents (eg, corticosteroids, immunoglobulins, other immune or cytokine-based therapies).
  • Previously stopped use of GLP-1RAs secondary to severe side effects including nausea, constipation, diarrhea, or emesis.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

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

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Part A Single-ascending Dose (SAD) in Healthy Participants

Participants will be randomized into 4 + (optional) 1 dose escalating cohorts and will receive GS-4571 or placebo to match (PTM) GS-4571 on Day 1, to determine the maximum tolerated dose:

  • Cohort 1: Dose 1 GS-4571, administered orally as a single dose, in a fasting state.
  • Cohort 2: Dose 2 GS-4571, administered orally as a single dose, in a fasting state.
  • Cohort 3: Dose 3 GS-4571, administered orally as a single dose, in a fasting state.
  • Cohort 4: Dose 4 GS-4571, administered orally as a single dose, in a fasting state.
  • Cohort 5 (optional): Dose 5 GS-4571, administered orally as a single dose, in a fasting state.

Administered orally

Administered orally

Eksperimentell: Part B Food/PPI Effect in Healthy Participants

Participants will be randomized into 2 sequence groups in Cohort 6 and will receive the highest dose found to be safe and well tolerated in Part A of GS-4571 and omeprazole. The two sequential groups will receive the following treatments:

  • Treatment A: Up to the highest single dose of GS-4571 evaluated in Part A, fasting.
  • Treatment B: Up to the highest single dose of GS-4571 evaluated in Part A, nonfasting (high-fat/high-calorie meal).
  • Treatment C (optional): Omeprazole, once-daily (QD) for 5 days, fasting.
  • Treatment D (optional): Omeprazole followed by up to the highest single dose of GS-4571 evaluated in Part A, 2 hours later, fasting.

Administered orally

Administered orally

Eksperimentell: Part C Multiple-ascending Dose (MAD) in Nondiabetic Obese Participants

Participants randomized in Cohorts 7-9 will be randomized to receive up to 4 escalating doses of GS-4571 or PTM QD for 12 weeks, as follows:

  • Cohort 7: Up to dose determined from Part A of GS-4571 or PTM in obese participants, QD, in a non-fasting state

  • Cohort 8: Up to 3-fold the Cohort 7 dose of GS-4571 or PTM in obese participants, QD, in a non-fasting state

  • Cohort 9: Up to 2-fold the Cohort 8 dose of GS-4571 or PTM in obese participants, QD, in a non-fasting state

  • Cohort 10 is optional and will receive GS-4571 or PTM QD for 12 weeks in case it is opened for enrollment as follows:

    • Up to 2-fold the Cohort 9 dose of GS-4571 or PTM in obese participants, QD, in a non-fasting state.

Administered orally

Administered orally

Eksperimentell: Part D Multiple Dose in Nonobese Participants With T2DM

Participants randomized in Cohort 11 will receive up to the highest dose of GS-4571 or PTM in T2DM, QD, in a non-fasting state for 12 weeks.

Administered orally

Administered orally

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Prosentandel av deltakere av behandlings-emergent adverse events (TEAE), alvorlige bivirkninger (SAE) eller dødsfall
Tidsramme: Dag 1 opptil 95 dager
Dag 1 opptil 95 dager
Prosentandel av deltakere av behandlingsoppståtte laboratorieavvik
Tidsramme: Dag 1 opptil 95 dager
Dag 1 opptil 95 dager
Single-Dose PK Parameter AUCinf of GS-4571
Tidsramme: Up to 96 hours postdose

AUCinf is defined as area under the concentration versus time curve extrapolated to infinite time.

Up to 96 hours postdose
Single-Dose PK Parameter Cmax of GS-4571
Tidsramme: Up to 96 hours postdose

Cmax is defined as the maximum observed concentration of drug in plasma.

Up to 96 hours postdose
Multiple-Dose Plasma PK Parameter: AUCtau of GS-4571
Tidsramme: Up to 96 hours postdose

AUCtau is defined as area under the concentration versus time curve over the dosing interval.

Up to 96 hours postdose
Multiple-Dose Plasma PK Parameter: Cmax of GS-4571
Tidsramme: Up to 96 hours postdose

Cmax is defined as the maximum observed concentration of drug in plasma.

Up to 96 hours postdose

Sekundære resultatmål

Resultatmål
Tidsramme
Prosentvis endring fra baseline (CFB) i kroppsvekt hos ikke-diabetiske overvektige deltakere
Tidsramme: Dag 1 opptil 95 dager
Dag 1 opptil 95 dager

Samarbeidspartnere og etterforskere

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

Sponsor

Etterforskere

  • Studieleder: Gilead Study Director, Gilead Sciences

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

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 (Faktiske)

28. august 2024

Primær fullføring (Antatt)

1. februar 2027

Studiet fullført (Antatt)

1. februar 2027

Datoer for studieregistrering

Først innsendt

16. august 2024

Først innsendt som oppfylte QC-kriteriene

16. august 2024

Først lagt ut (Faktiske)

20. august 2024

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. oktober 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

5. oktober 2026

Sist bekreftet

1. oktober 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • GS-US-506-6610

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

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. .