A Two-Part Single and Multiple Ascending Dose Trial of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LBT-3627 in Healthy Participants and in Participants With Parkinson's Disease.
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
30 – 89
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
64 (estimated)
Sponsor
Longevity Biotech Australia Pty Ltd (subsidiary) · Industry
Who this trial is looking for
This trial is looking for healthy adults and those with Parkinson's Disease to test a new treatment called LBT-3627. Participants will need to go through some medical assessments and receive doses of the study drug.
Are You a Good Fit for This Trial?
You may be able to join if
I am between 30 and 89 years old.
I have given written consent to participate.
I have a body mass index (BMI) between 18 and 32.
I have normal blood pressure and heart rate.
I have a normal body temperature.
I do not have any significant health issues based on my physical exam.
I am able to attend all scheduled visits and follow study procedures.
You may not be able to join if
I have used immunomodulators or coenzyme Q10 in the past 60 days.
I received a vaccine in the last 60 days.
I have a history of severe allergic reactions to medications.
I have had a stroke or unexplained loss of consciousness in the last year.
I have had a severe COVID-19 infection or 'Long-COVID'.
I have any major health disorder that could make the study unsafe.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Phase I a/b SAD/MAD study to evaluate safety and tolerability of LBT-3627 in both healthy volunteers and Parkinson's patients.
Trial Locations
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Status
Eligibility Criteria
Both cohorts (Healthy Volunteers and Parkinson's Disease)
Key inclusion criteria
* Male or female, 30-89 years inclusive at screening
* BMI 18-32 kg/m²
* Vital signs, ECG (QTcF \<450 ms male / \<470 ms female), and safety labs without clinically significant abnormality; no orthostatic hypotension
…
Both cohorts (Healthy Volunteers and Parkinson's Disease)
Key inclusion criteria
* Male or female, 30-89 years inclusive at screening
* BMI 18-32 kg/m²
* Vital signs, ECG (QTcF \<450 ms male / \<470 ms female), and safety labs without clinically significant abnormality; no orthostatic hypotension
* Women of non-childbearing potential, or using highly effective contraception per protocol
Key exclusion criteria
* Immunomodulators / steroids - HV: any (incl. OTC) within 90 days; PD: systemic within 60 days and topical/nasal-inhaled OTC within 7 days (both waivable only with Sponsor approval)
* Vaccine within 60 days (HV) / 45 days (PD) of first dose
* CoQ10 within 5 days
* Inadequate renal function (CrCl ≤ 60 mL/min; ≤ 79 if HV under 40), or LFTs / bilirubin \> 1.5× ULN
* Clinically significant cardiovascular, hepatic, renal, neurological, or psychiatric disease
* Active infection requiring systemic anti-infectives within 14 days; positive HBV/HCV/HIV serology
Parkinson's Disease participants - additional key inclusion criteria
* PD diagnosis by a neurologist/geriatrician, 6 months to \< 11 years before first dose, per MDS clinical diagnostic criteria
* Hoehn \& Yahr stage 1-3
* If on levodopa: stable ≥ 2 months and able to withhold ≥ 12 hours (overnight) around dosing/assessments; if not, remain treatment-naïve through end of study
Parkinson's Disease participants - additional key exclusion criteria
* Prior PD brain surgery, focused ultrasound, or neuromodulation; no anti-amyloid/anti-tau biologics
* Antibiotics within 30 days; OTC pre/probiotics; ≥ 3 unexplained falls in 12 months
Note: Additional protocol-defined criteria apply.
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