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

2026년 5월 25일 업데이트: 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.

연구 개요

상세 설명

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

연구 유형

중재적

등록 (추정된)

30

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Queensland
      • Brisbane, Queensland, 호주, 4006

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인

건강한 자원 봉사자를 받아들입니다

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 순차적 할당
  • 마스킹: 더블

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 코호트 1
Participants will be administered PMG1016 Dose 1 or placebo in a 100 mL IV infusion volume
다른 이름들:
  • PMG1016
실험적: 코호트 2
Participants will be administered PMG1016 Dose 2 or placebo in a 100 mL IV infusion volume
다른 이름들:
  • PMG1016
실험적: 코호트 3
Participants will be administered PMG1016 dose 3 or placebo in a 100 mL IV infusion volume
다른 이름들:
  • PMG1016
실험적: 코호트 4
Participants will be administered PMG1016 dose 4 or placebo in a 100 mL IV infusion volume
다른 이름들:
  • PMG1016

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Treatment-emergent adverse events (TEAEs)
기간: Day 1 to Day 57
The incidence and severity occurred
Day 1 to Day 57
Serious adverse events (SAEs)
기간: From Day 1 to Day 57
The incidence and severity occurred
From Day 1 to Day 57
Number of participants with abnormal pulse rate
기간: From Day 1 to Day 57
From Day 1 to Day 57
Number of participants with abnormal blood pressure
기간: From Day 1 to Day 57
From Day 1 to Day 57
Number of participants with abnormal respiratory rate
기간: From Day 1 to Day 57
From Day 1 to Day 57
Number of participants with abnormal tympanic temperature
기간: From Day 1 to Day 57
From Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal PR Interval
기간: From Day 1 to Day 57
From Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal QRS Duration
기간: From Day 1 to Day 57
From Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal QT interval
기간: From Day 1 to Day 57
From Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal RR interval
기간: From Day 1 to Day 57
From Day 1 to Day 57
Number of Participants with Clinically Significant Valvular Abnormalities
기간: 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
기간: 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
기간: Day 1 to Day 57
Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal Clinical Chemistry Results
기간: Day 1 to Day 57
Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal Urinalysis Results
기간: Day 1 to Day 57
Day 1 to Day 57
Number of Participants with Clinically Significant Abnormal Physical Examination Findings
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Incidence of anti-drug antibodies (ADA)
기간: 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)
기간: 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)
기간: 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)
기간: 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-∞)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 5월 22일

기본 완료 (추정된)

2026년 11월 30일

연구 완료 (추정된)

2026년 11월 30일

연구 등록 날짜

최초 제출

2026년 5월 10일

QC 기준을 충족하는 최초 제출

2026년 5월 25일

처음 게시됨 (실제)

2026년 5월 29일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 5월 29일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 5월 25일

마지막으로 확인됨

2026년 5월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

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아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

만성 신장 질환에 대한 임상 시험

PMG1016 Dose 1에 대한 임상 시험

구독하다