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A Study to Test the Safety and Blood Levels of PMG1016 in Healthy Adults

25. maj 2026 opdateret af: Pulmongene Ltd.

A Phase 1a, First-in-human, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of PMG1016 in Healthy Volunteers

This study is a first-in-human (FIH), randomized, double-blind, placebo-controlled study of PMG1016 in healthy adult participants. It aims to investigate the safety, tolerability, PK, and immunogenicity of PMG1016 administered via IV infusion.

Cohort 1: Healthy participants receiving single doses of PMG1016 Dose 1 or placebo.

Cohort 2: Healthy participants receiving single doses of PMG1016 Dose 2 or placebo.

Cohort 3: Healthy participants receiving single doses of PMG1016 Dose 3 or placebo.

Cohort 4: Healthy participants receiving single doses of PMG1016 Dose 4 or placebo.

Studieoversigt

Detaljeret beskrivelse

Participants will be enrolled and randomized into 1 of 4 cohorts in a double-blind manner

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

30

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Participants must be in good health based on medical history, physical exam, vital signs, ECG, and lab results at screening, as judged by the PI.
  • BMI 17.5-32.0 kg/m² and body weight 50-100 kg for males or 45-100 kg for females
  • No clinically significant lab abnormalities (hematology, coagulation, biochemistry, urinalysis) per PI discretion
  • Females: Must be non-pregnant, non-lactating, and use double contraception (condom + hormonal method/vaginal ring/IUD) through study completion, unless surgically sterile, postmenopausal, or in same-sex relationships. Negative pregnancy tests required. No oocyte donation for 90 days post dose.
  • Males: Must be surgically sterile, abstinent, or use condoms plus a highly effective method for female partners. Vasectomized males without proof of azoospermia must use condoms with WOCBP partners. No sperm donation for 90 days post dose.

Exclusion Criteria:

  • History or evidence of any clinically significant medical condition (e.g., cardiovascular, gastrointestinal, endocrine, hematologic, psychiatric, renal, musculoskeletal, infectious, neurological, or other major disease) as determined by the PI.
  • A PR <40 or >100 bpm or mean SBP >140 mmHg or DBP >95 mmHg (based on triplicate supine measurements after 5 minutes' rest).
  • Mean QTcF >450 ms (males) or >470 ms (females) at Screening; one repeat triplicate ECG allowed at PI discretion
  • Any clinically significant ECG abnormalities (rhythm, conduction, morphology) that may affect QTc interpretation, per PI judgment
  • ALT, AST, or creatinine >1.5 × ULN, or total bilirubin or lymphocytes > ULN.
  • Hemoglobin (HGB) below the lower limit of the normal range (ULN) prior to enrollment.
  • Participants with a positive toxicology screening panel or positive alcohol breath test at Screening and on Day -1.
  • Regular alcohol consumption defined as > 21 alcohol units per week. Participant is unwilling to abstain from alcohol beginning 48 hours prior to admission to the CRU and while residing at the CRU.
  • Blood donation or significant blood loss (≥500 mL) within 60 days prior to the first IP administration.
  • Plasma donation within 7 days prior to the first IP administration.
  • Use of any investigational product/device within 30 days or 5 half-lives (whichever is longer), or participation in >4 investigational drug studies in the past year.
  • Pregnant or lactating at Screening or planning pregnancy (self or partner) during the study or follow-up.
  • Fever >37.5°C or symptomatic infection within 2 weeks before Screening; any infection requiring systemic antibiotics within 3 months; history of recurrent infections; or a positive SARS-CoV-2 PCR before CRU admission.
  • Active malignancy, history of malignancy, or untreated precancerous lesions. Adequately treated or fully excised precancerous lesions are allowed.
  • Participants with a known history of retinal diseases, including conditions such as prior retinal detachment.
  • Participants with a history of recurrent epistaxis or gingival bleeding.
  • Use of prescription medications (except hormonal contraception) within 2 weeks before dosing; mAb products within 5 half-lives; or OTC drugs, supplements, or herbal products within 7 days before dosing.
  • History of anaphylaxis or severe allergy per PI judgment; mild untreated hay fever may be allowed.
  • History of allergic reaction or hypersensitivity to any of the excipients in the IP.
  • Positive screening test for HIV-1/2, HBsAg, HCV antibody, or syphilis.
  • Any condition that, in the PI's judgment, may pose a risk to the participant or the study.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Sekventiel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Kohorte 1
Participants will be administered PMG1016 Dose 1 or placebo in a 100 mL IV infusion volume
Andre navne:
  • PMG1016
Eksperimentel: Kohorte 2
Participants will be administered PMG1016 Dose 2 or placebo in a 100 mL IV infusion volume
Andre navne:
  • PMG1016
Eksperimentel: Kohorte 3
Participants will be administered PMG1016 dose 3 or placebo in a 100 mL IV infusion volume
Andre navne:
  • PMG1016
Eksperimentel: Kohorte 4
Participants will be administered PMG1016 dose 4 or placebo in a 100 mL IV infusion volume
Andre navne:
  • PMG1016

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Treatment-emergent adverse events (TEAEs)
Tidsramme: Day 1 to Day 57
The incidence and severity occurred
Day 1 to Day 57
Serious adverse events (SAEs)
Tidsramme: From Day 1 to Day 57
The incidence and severity occurred
From Day 1 to Day 57
Number of participants with abnormal pulse rate
Tidsramme: From Day 1 to Day 57
From Day 1 to Day 57
Number of participants with abnormal blood pressure
Tidsramme: From Day 1 to Day 57
From Day 1 to Day 57
Number of participants with abnormal respiratory rate
Tidsramme: From Day 1 to Day 57
From Day 1 to Day 57
Number of participants with abnormal tympanic temperature
Tidsramme: From Day 1 to Day 57
From Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal PR Interval
Tidsramme: From Day 1 to Day 57
From Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal QRS Duration
Tidsramme: From Day 1 to Day 57
From Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal QT interval
Tidsramme: From Day 1 to Day 57
From Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal RR interval
Tidsramme: From Day 1 to Day 57
From Day 1 to Day 57
Number of Participants with Clinically Significant Valvular Abnormalities
Tidsramme: Day 1 to Day 29
The number of participants with clinically significant valvular abnormalities identified by transthoracic echocardiography (TTE)
Day 1 to Day 29
Number of Participants with Clinically Significant Abnormal Left Ventricular Ejection Fraction
Tidsramme: Day 1 to Day 29
The number of participants with clinically significant abnormalities in left ventricular ejection fraction (LVEF) assessed by transthoracic echocardiography (TTE)
Day 1 to Day 29
Number of Participants with Clinically Significant Abnormal Hematology Results
Tidsramme: Day 1 to Day 57
Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal Clinical Chemistry Results
Tidsramme: Day 1 to Day 57
Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal Urinalysis Results
Tidsramme: Day 1 to Day 57
Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal Physical Examination Findings
Tidsramme: Day 1 to Day 57
assessment of general appearance; head; ears; eyes; nose; throat; dentition; thyroid; chest (heart and lungs); abdomen; skin; neurological system; extremities; back; neck; musculoskeletal system; and lymph nodes
Day 1 to Day 57

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Incidence of anti-drug antibodies (ADA)
Tidsramme: From Day 1 to Day 57
Percentage of PMG1016-induced ADA positive participants and percentage of PMG1016-boosted ADA positive participants
From Day 1 to Day 57
Maximum serum PMG1016 concentration (Cmax)
Tidsramme: Varying timepoints through end of treatment, up to Day 57
Determine PMG1016 Cmax in Serum
Varying timepoints through end of treatment, up to Day 57
Time to maximum concentration (Tmax)
Tidsramme: Varying timepoints through end of treatment, up to Day 57
Determine PMG1016 Tmax in Serum.
Varying timepoints through end of treatment, up to Day 57
Area under the serum drug concentration-time curve (AUC) from time zero to the last time point with measurable concentration (AUC0-t)
Tidsramme: Varying timepoints through end of treatment, up to Day 57
Determine PMG1016 AUC and AUC0-t in Serum.
Varying timepoints through end of treatment, up to Day 57
AUC from time zero to infinity (AUC0-∞)
Tidsramme: Varying timepoints through end of treatment, up to Day 57
Determine PMG1016 AUC0-∞ in Serum.
Varying timepoints through end of treatment, up to Day 57
The extrapolated portion of AUC0-∞ from Tlast to infinity (%AUCextrap)
Tidsramme: Varying timepoints through end of treatment, up to Day 57
Determine PMG1016 %AUCextrap in Serum.
Varying timepoints through end of treatment, up to Day 57
Terminal elimination half-life (t1/2)
Tidsramme: Varying timepoints through end of treatment, up to Day 57
Determine PMG1016 t1/2 in Serum.
Varying timepoints through end of treatment, up to Day 57
Apparent total body clearance (CL)
Tidsramme: Varying timepoints through end of treatment, up to Day 57
Determine PMG1016 CL in Serum.
Varying timepoints through end of treatment, up to Day 57
Apparent volume of distribution during the terminal phase (Vz)
Tidsramme: Varying timepoints through end of treatment, up to Day 57
Determine PMG1016 Vz in Serum.
Varying timepoints through end of treatment, up to Day 57
Apparent terminal elimination rate constant (λz)
Tidsramme: Varying timepoints through end of treatment, up to Day 57
Determine PMG1016 λz in Serum.
Varying timepoints through end of treatment, up to Day 57

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

22. maj 2026

Primær færdiggørelse (Anslået)

30. november 2026

Studieafslutning (Anslået)

30. november 2026

Datoer for studieregistrering

Først indsendt

10. maj 2026

Først indsendt, der opfyldte QC-kriterier

25. maj 2026

Først opslået (Faktiske)

29. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

29. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

25. maj 2026

Sidst verificeret

1. maj 2026

Mere information

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