NanO2 for Large Vessel Occlusion Stroke (PROVEN)

NuvOx Pharma

Status and phase: Not yet enrolling; Phase 3; Phase 2

Conditions: Ischemic Stroke

Treatments: Biological: dodecafluoropentane emulsion (DDFPe); Other: Placebo

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT05389748

PROVEN-P2

Details and patient eligibility

About

A two stage phase 2 study with an interim analysis to provide evidence that subjects provided with early administration of NanO2 who are located at small rural spoke hospitals and identified with large vessel occlusion ischemic strokes as well as viable penumbra prior to transfer to larger hub hospitals and who continue dosing NanO2 until revascularization is achieved by intravenous alteplase and/or mechanical thrombectomy, will experience stroke recovery by shifting ischemic brain tissue to normal tissue pO2 environments.

Full description

Recent stroke studies have shown that subjects with Large Vessel Occlusion (LVO) ischemic stroke have rapid infarct growth. The investigators hypothesize that early administration of NanO2 in subjects with LVO ischemic stroke will maintain the viability of tissue in the penumbra until revascularization is achieved with intravenous alteplase and/or mechanical thrombectomy (MT).

The rationale for administering the dose evaluated is:

1. The dose level is within the levels already tested in animals and humans.5-13 Volunteers received two IV bolus doses of 0.35 mL/kg of activated NanO2TM 24 hours apart and brain cancer subjects received daily doses of up to 0.17 mL/kg of inactivated NanO2TM.18
2. A completed trial of NanO2TM in acute ischemic stroke at the University of Arkansas had the high dose cohort receive three doses of NanO2 (0.17 mL/kg) 90 minutes apart and demonstrated safety at this dose.
3. Therapeutic reduction in stroke damage has been observed at dose levels of 0.1 mL/kg in rabbits.5-9,12 Since drug effects tend to correlate with body surface area/weight, one would predict that a dose of approximately 0.03 mL/kg should be effective in humans compared to rabbits.

Enrollment: 300 estimated patients

Sex: All

Ages: 18 to 90 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Ages 18 to 90 years old, male or female
• Diagnosis of LVO ischemic stroke
• Pre-stroke mRS ≤ 2
• NIHSS ≥ 6
• Eligible for mechanical thrombectomy per local criteria
• Subject or LAR must be willing and able to understand the study and provide written informed consent
• Women of childbearing potential or men with child-bearing potential partners (unless vasectomized) must agree to use a highly effective method of birth control from study entry until 4 months after completing study therapy. Should a study participant or their partner become pregnant or suspect a pregnancy they should inform the treating study physician immediately

Exclusion criteria

• > 12 hours since onset of stroke symptoms
• Currently pregnant or breastfeeding
• History of significantly impaired renal or hepatic function
• Severe hemorrhage or severe hemorrhagic stroke on CT scan. Mild or moderate changes of Fisher Grade 1 or 2 subarachnoid hemorrhage are allowed as are hemorrhagic transformation changes of Grade HI-1 and HI-224,25
• Unable to undergo a contrast brain perfusion scan with either MRI or CT
• Pre-stroke mRS > 2 (See Appendix 3)
• Unstable angina, NYHA Class II or greater congestive heart failure
• Uncontrolled hypertension (Systolic BP ≥ 200 and/or Diastolic BP ≤ 120 mmHg)
• Uncontrolled arrhythmia or history of clinically significant arrhythmia within the past six (6) months (except atrial fibrillation)
• Current acute or chronic lung disease requiring supplemental chronic or intermittent oxygen therapy.
• History of allergic reaction attributed to compounds of similar chemical composition to NanO2TM (see Investigator's Brochure).
• Subject has received any investigational drug within thirty (30) days prior to enrollment into the study
• Inability to comply with the study procedures
• History or evidence of any other clinically significant condition that, in the opinion of the investigator, might pose a safety risk to subjects or interfere with study procedures, evaluation, or completion

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

---

300 participants in 2 patient groups, including a placebo group

Placebo

Placebo Comparator group

Description:

Placebo which appears the same as the treatment to investigators, clinicians and subjects.

Treatment:

Other: Placebo

NanO2

Active Comparator group

Description:

A milky white intravenous injectable emulsion

Treatment:

Biological: dodecafluoropentane emulsion (DDFPe)