A Phase 1b Study to Assess the Safety and Tolerability of AB126 Neural Exosomes in Patients With Moderate to Severe Acute Ischemic Stroke

Prior treatment

• Pre-existing significant neurological deficits that would confound outcome assessments, including:
  • A pre-stroke modified Rankin Scale (mRS) score greater than 1
  • A history of prior stroke with persistent neurological deficits;
• Clinically significant stroke or head trauma within the previous 3 months, or residual neurological deficits from prior events that, in the opinion of the Investigator, would interfere with the assessment of clinical outcomes in the current study;
• Comorbidities that, in the judgment of the Investigator, would interfere with the ability to assess safety of the investigational product or the interpretation of study results. Such comorbidities may include, but are not limited to:
  • Active hepatic disease
  • Unstable angina or severe cardiovascular instability
  • Ongoing systemic infection
  • Allergy to human tissue
  • Restrictive pulmonary disease
  • Chronic lung infection
• Prior participation in a clinical interventional trial within the last 6 months;

Other illness

• Posterior circulation stroke, including infarcts involving brainstem or cerebellum;
• Clinically significant hemorrhagic transformation post-EVT, including:
  • PH-2 classification intracerebral hemorrhage (≥30% of infarcted area with significant mass effect)
  • sICH, as determined by the Investigator;
• Current clinically significant infection, including sepsis, meningitis, or active central nervous system infection;
• Recent history of seizures at stroke onset or a diagnosis of epilepsy;
• Known or suspected life expectancy less than 90 days due to non-stroke related comorbidities (e.g., advanced malignancy, end-stage organ failure);

Lab values

• Known sensitivity to bovine serum albumin or other components likely to be present in AB126;
• Patients with uncontrolled systemic medical conditions that may confound assessments or increase risk, including but not limited to:
  • Severe or unstable cardiovascular disease (e.g., recent myocardial infarction, uncontrolled arrhythmias)
  • Severe hepatic or renal disfunction (e.g., ALT/AST \>2x ULN, bilirubin \>1.5x ULN, or eGFR ≤30mL/min/1.73m2);
• Severe hyperglycemia or hypoglycemia at Screening, defined as blood glucose levels \<50 mg/dL or \>350 mg/dL. Participant may be eligible if glucose levels are stabilized during hospitalization prior to randomization, as assessed by the Investigator.

Other

• A \> ±30% change in NIHSS from Baseline to Pre-Randomization (i.e., 30% change in either direction)
• Comatose patients or those with severely reduced consciousness, defined as a score ≥2 on NIHSS Item 1a (Level of Consciousness) at the time of post-EVT assessment;
• Planned withdrawal of care or comfort measures only at the time of Screening;
• Women who are pregnant or nursing;
• Weight of ≥ 220 lbs.

• Male and female patients 18 to 85 years of age, inclusive.
• Provision of written informed consent obtained from participant or an acceptable legally authorized representative.
• Pre-stroke modified Rankin Scale score of 0 or 1.
• Diagnosis of AIS due to large vessel occlusion in the anterior circulation, confirmed by neuroimaging (NCCT, CTA).
• Diagnosis of moderate to severe cerebral ischemic stroke, defined by the presence of a measurable motor and/or speech-language deficit at pre-randomization, as assessed by the Investigator.
• Baseline National Institutes of Health Stroke Scale (NIHSS) score ≥12 prior to EVT to ensure sufficient stroke severity.
• Baseline imaging characteristics predictive of poor prognosis post-EVT defined by ASPECTS between 3 and 7 on NCCT.
• Has undergone EVT, specifically mechanical thrombectomy, for the treatment of the current AIS.
• Post-EVT NIHSS score, performed within 4 hours of EVT completion, must be between 12 and 25, inclusive, prior to randomization.
• Participants must demonstrate a change in NIHSS score of no more than ±30% from Baseline (pre-EVT) to Pre-Randomization (post-EVT).
• Patient must be capable of undergoing Magnetic Resonance Imaging (MRI).
• If male, participant must agree to use adequate contraceptive methods. If female, participant must be of non-childbearing potential or, if of childbearing potential, must agree to use adequate contraceptive methods.
• Patient must agree not to donate whole blood, blood components (including plasma and leukocytes), tissue, breast milk, ova, and sperm for one year following final administration of study drug.