Phase 1, Randomized, Double-blind, Placebo-controlled, Multiple-ascending-dose Trial to Evaluate the Safety, Tolerability, Immunogenicity, and Pharmacokinetics of Intravenous PNT001 in Hospitalized Patients With Traumatic Brain Injury (TBI)

Pinteon Therapeutics, Inc1 site in 1 country1 target enrollmentMarch 29, 2021

ConditionsTraumatic Brain Injury

Overview

Phase: Phase 1
Intervention: Not specified
Conditions: Traumatic Brain Injury
Sponsor: Pinteon Therapeutics, Inc
Enrollment: 1
Locations: 1
Primary Endpoint: Incidence of Treatment Emergent Adverse Events
Status: Terminated
Last Updated: 3 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

This is a Phase 1, multi-center, randomized, double-blind, placebo-controlled, multiple-ascending- dose trial to evaluate the safety, tolerability, immunogenicity, and pharmacokinetics of intravenous PNT001 in hospitalized patients with traumatic brain injury.

Detailed Description

The Phase 1 study is a double-blind, multiple ascending dose trial evaluating a total of 64 patients across two dose cohort groups. Each cohort will include 32 patients (24 active; 8 placebo) who will be randomized to receive three doses of either PNT001 or placebo. Doses studied will be 1000mg and 4000mg. Patients admitted to the trauma center who meet entrance criteria will receive their first dose of study drug within 24 hours of documented TBI. They will remain in the facility for at least 24 hours after initial dose. Baseline biomarker collection and cognitive assessments will be completed. Study medication will be administered as an IV infusion over 30 minutes (for 1000mg cohort) or 60 minutes (for 4000mg cohort) followed by collection of safety, tolerability, pharmacokinetic, biomarker, imaging, and cognitive data over 12 weeks. Subsequent dosing visits will be at Days 28 and 56. All visits after initial discharge will be on an outpatient basis.

Registry

clinicaltrials.gov

Start Date

March 29, 2021

End Date

April 12, 2021

Last Updated

3 years ago

Study Type

Interventional

Study Design

Sequential

Sex

All

Investigators

Sponsor

Pinteon Therapeutics, Inc

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Hospitalization due to documented evidence of TBI with Glasgow Coma Scale (GCS) Score 9-12 or GCS score of 13-15 with radiographic evidence of trauma.
•Duration from documented time of TBI event to time of start of initial dose of study drug will not exceed 24 hours.
•Signed informed consent by patient, or where applicable, patient's legally authorized representative.
•Male and females, 18- 65 years of age at time of screening (State's legal age of majority is minimum age if higher than 18).
•Female patients must meet protocol defined criteria for 1) non-childbearing potential, 2) post menopausal or 3) must have a negative pregnancy test and agree to contraception as outlined in the protocol.
•Male must agree to use acceptable contraception and refrain from sperm donation during the entire study and for 200 days after dosing has been completed.
•Has not participated in a clinical drug trial within 3 months of study start.
•Body Mass Index (BMI) of 18.5-35.0 kg/m2 and for the 4000mg dose group only, weight greater than or equal to 44.8 kg.
•Vision, hearing, speech, motor function, and comprehension sufficient for compliance with all testing procedures and assessments.

Exclusion Criteria

•TBI that does not require hospitalization.
•TBI outside 24-hour window.
•GCS \< 9 within 2 hours of dosing.
•History of TBI in past 12 months that resulted in patient seeking medical attention.
•Evidence of penetrating head trauma or depressed skull fracture.
•Clinical or radiographic evidence of mass effect, midline shift, or intracranial hypertension, requiring craniotomy/craniectomy.
•Evidence of symptomatic cervical, thoracic, lumbar spine injury e.g. paresis, radiculopathy, that can be localized to the injury.
•Systemic traumatic injury that would preclude participation in study or is expected to result in long-term disability.
•Any other acute or chronic medical illness that in the judgement of the study physician results in functional impairment or impairs neuropsychiatric function.
•Any acute intoxication that in the judgement of the study physician results in significant functional impairment or impairs neuropsychiatric function.