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A Study to Evaluate the Safety and Pharmacokinetics of AZD7760 in Healthy Japanese Adults

17. august 2026 oppdatert av: AstraZeneca

A Phase I, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Pharmacokinetics of AZD7760 in Healthy Japanese Adult Participants

The purpose of this study is to evaluate the safety and PK of AZD7760 when given as an intravenous (IV) infusion to healthy Japanese adult participants.

Studieoversikt

Status

Rekruttering

Intervensjon / Behandling

Detaljert beskrivelse

This is a Phase I, randomized, double-blind, placebo-controlled, dose escalation study to evaluate the safety and PK of AZD7760, a mAb combination of suvratoxumab (labeled as MEDI4893) and AZD7745, in healthy Japanese adults. Two dosages of AZD7760 each administered as a single IV dose, will be assessed.

Study details include:

  • A Screening Period of up to 28 days.
  • A Dosing Period of 3 days, in which a single IV infusion will be given on Day 1.
  • A Follow-up Period of 12 months from the time of administration of the study intervention.

Studietype

Intervensjonell

Registrering (Antatt)

18

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

      • Sumida-ku, Japan, 130-0004
        • Rekruttering
        • Research Site

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:

  • Body weight ≥ 45 kg and ≤ 110 kg and BMI within the range of ≥ 18.0 to ≤ 30.0 kg/m2 (inclusive) at screening.
  • Healthy Japanese participants with no clinically significant concomitant diseases or medications.

Exclusion Criteria:

  • Known hypersensitivity to any component of the study intervention.
  • Previous hypersensitivity, infusion-related reaction, or severe adverse reaction following administration of mAbs.
  • Clinically significant bleeding disorder or prior history of significant bleeding or bruising following intramuscular injections or venipuncture.
  • AST or ALT above 1.5 × ULN at screening.
  • Estimated glomerular filtration rate < 90 mL/min/1.73 m2.
  • Hemoglobin or platelet count below the lower limit of normal at screening.
  • White blood cell counts outside normal reference ranges.
  • History of malignancy other than treated non-melanoma skin cancers or locally treated cervical cancer in the previous 5 years.
  • Any clinically significant abnormalities on 12-lead ECG at screening,
  • Acute (time-limited) illness, including fever ≥ 38 °C (100.4 °F), one day prior to or on the day of planned dosing.
  • Known or suspected congenital or acquired immunodeficiency, or receipt of immunosuppressive therapy.
  • Any condition that has the potential to increase clearance of the study intervention.
  • Blood donation or collection as follows:

    1. 400 mL whole blood donation within 12 weeks (males) or 16 weeks (females) prior to study drug administration.
    2. 200 mL whole blood donation within 4 weeks prior to study drug administration.
    3. Apheresis donation within 2 weeks prior to study drug administration.
  • Absence of suitable veins for blood sampling and administration of study intervention.
  • Any other condition that would compromise the safety of the participants.
  • Any condition that might interfere with evaluation of the study intervention or interpretation of participant safety or study results.
  • Any laboratory value in the screening panel that, in the opinion of the investigator, is clinically significant or might confound analysis of study results. Testing may be repeated once at the investigator's discretion.

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

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

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Cohort 1 (AZD7760 Dose A)
Participants receive an IV infusion of AZD7760 Dose A on Day 1.
Participants will receive AZD7760 via IV infusion.
Eksperimentell: Cohort 2 (AZD7760 Dose B)
Participants receive an IV infusion of AZD7760 Dose B on Day 1.
Participants will receive AZD7760 via IV infusion.
Placebo komparator: Pooled Placebo
Participants receive an IV infusion of matching placebo on Day 1.
Participants will receive matching placebo via IV infusion.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Occurrence of Adverse Events (AEs)
Tidsramme: Day 1 to Day 181
To evaluate the safety of AZD7760 administered as a single IV Dose A or Dose B in healthy Japanese adult participants.
Day 1 to Day 181
Occurrence of Medically-attended Adverse Events (MAAEs), Serious Adverse Events (SAEs), and Adverse Events of Special Interest (AESIs)
Tidsramme: Day 1 to Day 361
To evaluate the safety of AZD7760 administered as a single IV Dose A or Dose B in healthy Japanese adult participants.
Day 1 to Day 361

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Maximum observed serum (peak) drug concentration (Cmax)
Tidsramme: Day 1 to Day 361
To characterize the PK of AZD7760 in serum of healthy Japanese adult participants.
Day 1 to Day 361
Time to reach peak or maximum observed concentration following drug administration (tmax)
Tidsramme: Day 1 to Day 361
To characterize the PK of AZD7760 in serum of healthy Japanese adult participants.
Day 1 to Day 361
Terminal elimination half-life (t½λz)
Tidsramme: Day 1 to Day 361
To characterize the PK of AZD7760 in serum of healthy Japanese adult participants.
Day 1 to Day 361
Area under the concentration-time curve from time 0 to the time of the last quantifiable concentration (AUClast)
Tidsramme: Day 1 to Day 361
To characterize the PK of AZD7760 in serum of healthy Japanese adult participants.
Day 1 to Day 361
Area under the concentration-time curve from time 0 to infinity (AUCinf)
Tidsramme: Day 1 to Day 361
To characterize the PK of AZD7760 in serum of healthy Japanese adult participants.
Day 1 to Day 361
Volume of distribution at steady state (Vss)
Tidsramme: Day 1 to Day 361
To characterize the PK of AZD7760 in serum of healthy Japanese adult participants.
Day 1 to Day 361
Volume of distribution based on the terminal phase (Vz)
Tidsramme: Day 1 to Day 361
To characterize the PK of AZD7760 in serum of healthy Japanese adult participants.
Day 1 to Day 361
Incidence of Anti-drug antibody (ADA)
Tidsramme: Day 1 to Day 361
To evaluate ADA responses to AZD7760 in serum of healthy Japanese adult participants
Day 1 to Day 361

Samarbeidspartnere og etterforskere

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

Sponsor

Samarbeidspartnere

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)

29. juni 2026

Primær fullføring (Antatt)

13. september 2027

Studiet fullført (Antatt)

13. september 2027

Datoer for studieregistrering

Først innsendt

21. mai 2026

Først innsendt som oppfylte QC-kriteriene

21. mai 2026

Først lagt ut (Faktiske)

29. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

18. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

17. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • D7480C00003

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-planbeskrivelse

Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal Vivli.org. All requests will be evaluated as per the AZ disclosure commitment: https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure. ''Yes", indicates that AZ is accepting requests for IPD, but this does not mean all requests will be approved.

IPD-delingstidsramme

AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA/PhRMA Data-Sharing Principles. For details of our timelines, please refer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

Tilgangskriterier for IPD-deling

When a request has been approved AstraZeneca will provide access to the anonymized individual patient-level data via secure research environment Vivli.org. A Signed Data Usage Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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