A Study to Test the Safety and Blood Levels of PMG1016 in Healthy Adults
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.
Studieöversikt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljerad beskrivning
Studietyp
Studietyp
Inskrivning (Beräknad)
Inskrivning
Fas
Fas
- Fas 1
Kontakter och platser
Studiekontakt
Studiekontakt
- Namn: Yaohui Wang
- Telefonnummer: +86 13810669548
- E-post: yaohui_wang@pulmongene.com
Studieorter
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Queensland
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Brisbane, Queensland, Australien, 4006
- Nucleus Network (Brisbane)
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Kontakt:
- Richard Friend, Dr
- Telefonnummer: (07) 3707 2720
- E-post: r.friend@nucleusnetwork.com.au
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Deltagandekriterier
Urvalskriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
Tar emot friska volontärer
Beskrivning
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
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Sekventiell tilldelning
- Maskning: Dubbel
Antal vapen
Vapen och interventioner
Deltagargrupp / ArmDeltagargrupp / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
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Experimentell: Kohort 1
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Participants will be administered PMG1016 Dose 1 or placebo in a 100 mL IV infusion volume
Andra namn:
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Experimentell: Kohort 2
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Participants will be administered PMG1016 Dose 2 or placebo in a 100 mL IV infusion volume
Andra namn:
|
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Experimentell: Kohort 3
|
Participants will be administered PMG1016 dose 3 or placebo in a 100 mL IV infusion volume
Andra namn:
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Experimentell: Kohort 4
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Participants will be administered PMG1016 dose 4 or placebo in a 100 mL IV infusion volume
Andra namn:
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Vad mäter studien?
Primära resultatmått
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Treatment-emergent adverse events (TEAEs)
Tidsram: Day 1 to Day 57
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The incidence and severity occurred
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Day 1 to Day 57
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Serious adverse events (SAEs)
Tidsram: From Day 1 to Day 57
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The incidence and severity occurred
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From Day 1 to Day 57
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Number of participants with abnormal pulse rate
Tidsram: From Day 1 to Day 57
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From Day 1 to Day 57
|
|
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Number of participants with abnormal blood pressure
Tidsram: From Day 1 to Day 57
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From Day 1 to Day 57
|
|
|
Number of participants with abnormal respiratory rate
Tidsram: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of participants with abnormal tympanic temperature
Tidsram: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal PR Interval
Tidsram: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal QRS Duration
Tidsram: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal QT interval
Tidsram: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal RR interval
Tidsram: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Valvular Abnormalities
Tidsram: Day 1 to Day 29
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The number of participants with clinically significant valvular abnormalities identified by transthoracic echocardiography (TTE)
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Day 1 to Day 29
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Number of Participants with Clinically Significant Abnormal Left Ventricular Ejection Fraction
Tidsram: Day 1 to Day 29
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The number of participants with clinically significant abnormalities in left ventricular ejection fraction (LVEF) assessed by transthoracic echocardiography (TTE)
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Day 1 to Day 29
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Number of Participants with Clinically Significant Abnormal Hematology Results
Tidsram: Day 1 to Day 57
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Day 1 to Day 57
|
|
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Number of Participants with Clinically Significant Abnormal Clinical Chemistry Results
Tidsram: Day 1 to Day 57
|
Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal Urinalysis Results
Tidsram: Day 1 to Day 57
|
Day 1 to Day 57
|
|
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Number of Participants with Clinically Significant Abnormal Physical Examination Findings
Tidsram: Day 1 to Day 57
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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
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Day 1 to Day 57
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Sekundära resultatmått
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Incidence of anti-drug antibodies (ADA)
Tidsram: From Day 1 to Day 57
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Percentage of PMG1016-induced ADA positive participants and percentage of PMG1016-boosted ADA positive participants
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From Day 1 to Day 57
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Maximum serum PMG1016 concentration (Cmax)
Tidsram: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 Cmax in Serum
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Varying timepoints through end of treatment, up to Day 57
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Time to maximum concentration (Tmax)
Tidsram: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 Tmax in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Area under the serum drug concentration-time curve (AUC) from time zero to the last time point with measurable concentration (AUC0-t)
Tidsram: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 AUC and AUC0-t in Serum.
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Varying timepoints through end of treatment, up to Day 57
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AUC from time zero to infinity (AUC0-∞)
Tidsram: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 AUC0-∞ in Serum.
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Varying timepoints through end of treatment, up to Day 57
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The extrapolated portion of AUC0-∞ from Tlast to infinity (%AUCextrap)
Tidsram: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 %AUCextrap in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Terminal elimination half-life (t1/2)
Tidsram: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 t1/2 in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Apparent total body clearance (CL)
Tidsram: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 CL in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Apparent volume of distribution during the terminal phase (Vz)
Tidsram: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 Vz in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Apparent terminal elimination rate constant (λz)
Tidsram: Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 λz in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Samarbetspartners och utredare
Sponsor
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Beräknad)
Studiestart
Primärt slutförande (Beräknad)
Primärt slutförande
Avslutad studie (Beräknad)
Avslutad studie
Studieregistreringsdatum
Först inskickad
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Första postat
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste uppdatering publicerad
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
- Urogenitala sjukdomar
- Patologiska processer
- Manliga urogenitala sjukdomar
- Njursjukdomar
- Urologiska sjukdomar
- Kvinnliga urogenitala sjukdomar
- Kvinnliga urogenitala sjukdomar och graviditetskomplikationer
- Kronisk sjukdom
- Sjukdomsegenskaper
- Njurinsufficiens
- Patologiska tillstånd, tecken och symtom
- Njurinsufficiens, kronisk
Andra studie-ID-nummer
Andra studie-ID-nummer
- PMG1016-1031
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Läkemedels- och apparatinformation, studiedokument
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