Safety and Tolerability of PNT001 in Patients With Acute Traumatic Brain Injury (TBI)

This is an interventional treatment trial for Traumatic Brain Injury Read More

Inclusion Criteria:

1. 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.
2. Duration from documented time of TBI event to time of start of initial dose of study drug will not exceed 24 hours.
3. Signed informed consent by patient, or where applicable, patient's legally authorized representative.
4. 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).
5. 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.
6. 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.
7. Has not participated in a clinical drug trial within 3 months of study start.
8. 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.
9. Vision, hearing, speech, motor function, and comprehension sufficient for compliance with all testing procedures and assessments.

Exclusion Criteria:

1. TBI that does not require hospitalization.
2. TBI outside 24-hour window.
3. GCS < 9 within 2 hours of dosing.
4. History of TBI in past 12 months that resulted in patient seeking medical attention.
5. Evidence of penetrating head trauma or depressed skull fracture.
6. Clinical or radiographic evidence of mass effect, midline shift, or intracranial hypertension, requiring craniotomy/craniectomy.
7. Evidence of symptomatic cervical, thoracic, lumbar spine injury e.g. paresis, radiculopathy, that can be localized to the injury.
8. Systemic traumatic injury that would preclude participation in study or is expected to result in long-term disability.
9. Any other acute or chronic medical illness that in the judgement of the study physician results in functional impairment or impairs neuropsychiatric function.
10. Any acute intoxication that in the judgement of the study physician results in significant functional impairment or impairs neuropsychiatric function.
11. Any history of cancer within 5 years of enrollment with the exception of resected skin basal cell carcinoma.
12. Any major surgery requiring general anesthesia within 4 weeks of study drug administration.
13. Donation of blood or serum ≥500 mL to a blood bank or in a clinical study (except screening visit) within 3 months of study drug administration.
14. Known recent (within 6 months of study drug administration) drug or alcohol abuse as defined in DSM V, Diagnostic Criteria for Drug and Alcohol Abuse.
15. Evidence of any clinically significant neurological or psychiatric disorder that could interfere with study assessments as determined by investigator and sponsor.
16. Patient has history or currently has schizophrenia, schizoaffective disorder or bipolar disorder, untreated major depression (DSM-V or ICD-10 criteria).
17. Significant illness within the prior 30 days.
18. Abnormalities in creatinine, hepatic transaminases, or QT that would preclude entry into the study.