Fortrea Clinical Research Unit Inc.
Dallas, Texas, 75230, United States
NCT Number: NCT07518771
This was a double blind, randomized, placebo controlled, single and multiple IV dose study conducted in 2 parts, single ascending dose and multiple ascending doses parts. The principal aim of this study was to obtain safety and tolerability data when PA-001 is administered IV as single and multiple doses to healthy subjects. This information, together with the PK data, will help establish the doses and dosing regimen suitable for future studies in patients. The study also investigated the effects of age on the PK of PA-001 prior to patient studies.
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Notify Me18 year and older
All sexes
Interventional
Phase 1
Dallas, Texas, 75230, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
PA-001 or Placebo was infused via IV in accordance with a randomized schedule, after a fast of at least 10 hours
Time frame: For approx. 8 weeks
An adverse event (AE) was any untoward medical occurrence in a subject, temporally associated with the use of study intervention. A serious adverse event (SAE) was defined as any untoward medical occurrence that, at any dose, met one or more of the following criteria: resulted in death, was life-threatening, required inpatient hospitalization or prolongation of existing hospitalization, resulted in persistent or significant disability/incapacity, resulted in a congenital anomaly/birth defect and resulted in an important medical events. TEAEs were defined as events that occurred after start of treatment.
Time frame: For approx. 8 weeks
Clinical hematology parameters included: hemoglobin, hematocrit, red blood cell count, platelet count, white blood cell count, total neutrophils, eosinophils, monocytes, basophils, lymphocytes, mean cell hemoglobin (MCH), MCH concentration and mean cell volume.
Chemistry parameters included: blood urea nitrogen, creatinine, estimated glomerular filtration rate, glucose, calcium, sodium, potassium, chloride, aspartate aminotransferase, alanine aminotransferase, total bilirubin, alkaline phosphatase, uric acid, albumin, total protein, bicarbonate, gamma-glutamyl transferase, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, B-type natriuretic peptide, highly sensitive troponin T and lactate dehydrogenase.
Urinalysis parameters included: potential of hydrogen (pH), glucose, protein, blood, ketones, nitrite, leukocyte esterase, bilirubin, color and appearance, specific gravity.
Time frame: For approx. 8 weeks
A 12-lead ECG was performed. Clinically meaningful findings in ECG assessments were based on the investigator's judgment
Time frame: SAD: predose to 48 hours after start of infusion, MAD: predose to 48 hours after start of the last infusion
AUCinf was calculated as AUClast + (Clast/kel) where Clast was the predicted plasma concentration at the last quantifiable time point from the log-linear regression analysis and kel was the terminal phase rate constant calculated by a linear regression of the log linear concentration-time curve
Time frame: SAD: predose to 48 hours after start of infusion, MAD: predose to 48 hours after start of the last infusion
AUClast was calculated as area under the concentration time curve from time 0 to the time of the last quantifiable concentration
Time frame: SAD: predose to 48 hours after start of infusion, MAD: predose to 48 hours after start of the last infusion
Cmax was maximum observed concentration. Cmax was observed directly from data
Time frame: SAD: predose to 48 hours after start of infusion, MAD: predose to 48 hours after start of the last infusion
T1/2 was terminal elimination half life
Time frame: SAD only, predose to 48 hours after start of infusion
Percentage of the dose administered recovered over the time interval, 0 hour to the end of collection
PeptiDream Inc.
Industry
PA-001 - A Phase 1, Double Blind, Randomized, Placebo Controlled, Single and Multiple Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics in Healthy and Elderly Subjects
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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