Overview
Study to Assess the Safety and Efficacy of Sovateltide in Patients With Acute Cerebral Ischemic Stroke
Status:
Recruiting
Recruiting
Trial end date:
2025-07-01
2025-07-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This is a prospective, multicenter, randomized, double-blind, parallel, phase IV study designed to evaluate the safety and efficacy of sovateltide (PMZ-1620, IRL-1620) as a potential treatment for cerebral ischemic stroke.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Pharmazz, Inc.
Criteria
Inclusion Criteria:- Adult males or females aged 18 years through 78 years (have not had their 79th
birthday)
- Patient or Legally Acceptable Representative (LAR) willing to give informed consent
before study procedure.
- Stroke is ischemic in origin and radiologically confirmed Computed Tomography (CT)
scan or diagnostic magnetic resonance imaging (MRI) before enrolment. No hemorrhage as
proved by cerebral CT/MRI scan.
- Cerebral ischemic stroke patients presenting within 24 hours after onset of symptoms
with mRS score of 3-4 (pre-stroke mRS score of 0 or 1) and NIHSS score >5 (NIHSS Level
of Consciousness (1A) score must be < 2). This includes cerebral ischemic stroke
patients who completely recovered from earlier episodes before having a new or fresh
stroke.
- The patient is <24 hours from the time of stroke onset when the first dose of
Sovateltide therapy is administered. Time of onset is when symptoms began; for stroke
that occurred during sleep, time of onset is when the patient was last seen or was
self-reported to be normal.
- Reasonable expectation of availability to receive the full Sovateltide course of
therapy and to be available for subsequent follow-up visits.
Exclusion Criteria:
- Patients receiving endovascular therapy or is a candidate for any surgical
intervention for the treatment of stroke, which may include but not limited to
endovascular techniques.
- Patients classified as comatose are defined as a patient who requires repeated
stimulation to attend or is obtunded and requires strong or painful stimulation to
make movements (NIHSS Level of Consciousness (1A) score ≥ 2).
- Evidence of intracranial hemorrhage (intracerebral hematoma, intraventricular
hemorrhage, subarachnoid hemorrhage, epidural hemorrhage, an acute or chronic subdural
hematoma on the baseline CT or MRI scan 4. Known pregnancy.
- Confounding pre-existing neurological or psychiatric disease.
- Concurrent participation in any other therapeutic clinical trial.
- Evidence of any other major life-threatening or serious medical condition that would
prevent completion of the study protocol, impair the assessment of outcome, or in
which Sovateltide therapy would be contraindicated or might cause harm to the patient.