- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07615985
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.
Přehled studie
Postavení
Podmínky
Intervence / Léčba
Detailní popis
Typ studie
Zápis (Odhadovaný)
Fáze
- Fáze 1
Kontakty a umístění
Studijní kontakt
- Jméno: Yaohui Wang
- Telefonní číslo: +86 13810669548
- E-mail: yaohui_wang@pulmongene.com
Studijní místa
-
-
Queensland
-
Brisbane, Queensland, Austrálie, 4006
- Nucleus Network (Brisbane)
-
Kontakt:
- Richard Friend, Dr
- Telefonní číslo: (07) 3707 2720
- E-mail: r.friend@nucleusnetwork.com.au
-
-
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
Přijímá zdravé dobrovolníky
Popis
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.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Randomizované
- Intervenční model: Sekvenční přiřazení
- Maskování: Dvojnásobek
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: Kohorta 1
|
Participants will be administered PMG1016 Dose 1 or placebo in a 100 mL IV infusion volume
Ostatní jména:
|
|
Experimentální: Kohorta 2
|
Participants will be administered PMG1016 Dose 2 or placebo in a 100 mL IV infusion volume
Ostatní jména:
|
|
Experimentální: Kohorta 3
|
Participants will be administered PMG1016 dose 3 or placebo in a 100 mL IV infusion volume
Ostatní jména:
|
|
Experimentální: Kohorta 4
|
Participants will be administered PMG1016 dose 4 or placebo in a 100 mL IV infusion volume
Ostatní jména:
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Treatment-emergent adverse events (TEAEs)
Časové okno: Day 1 to Day 57
|
The incidence and severity occurred
|
Day 1 to Day 57
|
|
Serious adverse events (SAEs)
Časové okno: From Day 1 to Day 57
|
The incidence and severity occurred
|
From Day 1 to Day 57
|
|
Number of participants with abnormal pulse rate
Časové okno: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of participants with abnormal blood pressure
Časové okno: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of participants with abnormal respiratory rate
Časové okno: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of participants with abnormal tympanic temperature
Časové okno: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal PR Interval
Časové okno: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal QRS Duration
Časové okno: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal QT interval
Časové okno: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal RR interval
Časové okno: From Day 1 to Day 57
|
From Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Valvular Abnormalities
Časové okno: 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
Časové okno: 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
Časové okno: Day 1 to Day 57
|
Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal Clinical Chemistry Results
Časové okno: Day 1 to Day 57
|
Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal Urinalysis Results
Časové okno: Day 1 to Day 57
|
Day 1 to Day 57
|
|
|
Number of Participants with Clinically Significant Abnormal Physical Examination Findings
Časové okno: 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
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Incidence of anti-drug antibodies (ADA)
Časové okno: 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)
Časové okno: 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)
Časové okno: 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)
Časové okno: 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-∞)
Časové okno: 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)
Časové okno: 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)
Časové okno: 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)
Časové okno: 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)
Časové okno: 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)
Časové okno: 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
|
Spolupracovníci a vyšetřovatelé
Sponzor
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
- Urogenitální onemocnění
- Patologické procesy
- Mužská urogenitální onemocnění
- Onemocnění ledvin
- Urologická onemocnění
- Ženské urogenitální onemocnění
- Ženské urogenitální onemocnění a těhotenské komplikace
- Chronické onemocnění
- Atributy nemoci
- Renální insuficience
- Patologické stavy, příznaky a symptomy
- Renální insuficience, chronická
Další identifikační čísla studie
- PMG1016-1031
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .
Klinické studie na PMG1016 Dose 1
-
Riphah International UniversityDokončenoPevnost hamstringůPákistán
-
Tang-Du HospitalJiangsu Hengrui Pharmaceutical Co., Ltd.NáborRakovina žaludkuČína
-
Ohio State UniversityUkončenoDiabetes mellitus, typ 2 | Glukóza v krvi, vysoká | Propuštění pacienta | Hladina glukózy v krvi, nízkáSpojené státy
-
University Hospital, Clermont-FerrandDokončenoChronická bolest dolní části zadFrancie
-
Hallym University Medical CenterSanofi; Asan Medical CenterDokončenoNovotvary žaludkuKorejská republika
-
Aalborg University HospitalAalborg UniversityDokončenoDiabetes | Svalová slabost | Sarkopenie | Diabetická periferní neuropatie | Zůstatek; Zkreslený | Neuropatie malých vláken | Autonomní neuropatie, diabetes | Vestibulární neuropatieDánsko
-
University of Sao Paulo General HospitalDokončeno
-
Orasis Pharmaceuticals Ltd.DokončenoPresbyopieSpojené státy
-
University of ThessalyDokončeno
-
University of Sao Paulo General HospitalDokončenoSyndrom hyperaktivního močového měchýřeBrazílie