A Multi-Center, Randomized, Double-Blind, Parallel, Placebo-Controlled, Phase III Clinical Study to Evaluate Efficacy and Safety of SP-8203 (Otaplimastat) in Patients With Acute Ischemic Stroke Requiring Thrombolytic Therapy as Standard of Care

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

This clinical study is designed to evaluate the efficacy and safety of the combination therapy of SP-8203 (otaplimastat) and thrombolytic standard of care in acute ischemic stroke patient. As a standard of care, thrombolytic therapy (for instance, recombinant tissue plasminogen activator) will be administered. When reperfusion is not achieved in spite of thrombolytic therapy, endovascular therapy can be performed.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Maximum Age: 85
Healthy Volunteers: f
View:

• Patients with neurologic deficit of ≥ 8 points by National Institute of Health Stroke Scale (NIHSS) score

• Patients with pre-stroke modified Rankin Scale (mRS) must be 0 or 1, which means they were able to carry out all usual duties and activities

• Adults aged ≥19 years and ≤85 years

• Patients who can receive thrombolytic standard of care within 4.5 hours after the onset of early symptoms of acute ischemic stroke

• Patients available for brain Magnetic Resonance Imaging (MRI) scanning

• Patients who consent to participate in this study

Locations
Other Locations
Republic of Korea
Dong-A University Hospital
RECRUITING
Busan
Ulsan University Hospital
RECRUITING
Ulsan
Contact Information
Primary
Jong Sung Kim, MD, Phd
jongskim@amc.seoul.kr
+82-33-610-3114
Backup
Byung Su Kim, MS
135kbs@shinpoong.co.kr
+82-70-5168-6503
Time Frame
Start Date: 2025-02-14
Estimated Completion Date: 2027-03-30
Participants
Target number of participants: 852
Treatments
Experimental: SP-8203
SP-8203 80 mg (40 mg/dose twice a day for three days)
Placebo_comparator: Placebo
Placebo group: twice a day for three days
Related Therapeutic Areas
Sponsors
Leads: Shin Poong Pharmaceutical Co. Ltd.

This content was sourced from clinicaltrials.gov

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