Safety and Efficacy of Two Doses of SP-8203 in Patients With Ischemic Stroke Requiring rtPA (SP-8203-2001)

July 20, 2020 updated by: Shin Poong Pharmaceutical Co. Ltd.

A Prospective, Randomized, Double-blinded Phase IIa Clinical Trial to Investigate the Safety and Efficacy of Two Doses of SP-8203 in Patients With Ischemic Stroke Requiring rtPA Standard of Care

The current study aims to evaluate the safety of SP-8203, designing in two stages (stage-1, stage-2) to evaluate the safety and efficacy of the combination therapy of SP-8203 and rtPA for the occurrence of cerebral hemorrhage in patients with acute ischemic stroke receiving rtPA standard of care.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

As the standard procedure of rtPA therapy, rtPA will be injected intravenously using a device like infusion pump. When reperfusion is not achieved in spite of rtPA therapy, endovascular therapy can be performed according to the judgment of a site investigator.

Stage 1-The trial will be conducted with 11 subjects participating in an open label design manner. Subjects with neurologic deficit of ≥4 point and ≤10 points on NIHSS score will be given SP-8203, 80mg/dose, a total of 6 times at intervals of 12 hours. For the first administration of SP-8203, it should be administered within 30 minutes from the initiation of rtPA administration via a vein route different from one via which rtPA is injected.

Thereafter, the subject will be transferred to MRI scanning room to have brain MRI and MRA performed, and brain CT will be performed to check the occurrence of intracranial hemorrhage at 24 hours after complete administration of the first dose of SP-8203. The subject will be closely monitored by research staff daily from the day of first administration of SP-8203 (Day 0) to Day 5. Brain MRI and MRA will be followed up after the last administration of SP-8203 on Day 5. The subject will make a visit on Day 14 to have his/her neurologic symptoms checked, after which subject's participation in the trial will be completed.

*The DSMB (Date Safety Monitoring Board) meeting will be held, to decide whether to proceed with Stage 2 or not, based on the results of Stage 1.

Stage 2- A total of 69 subjects will be enrolled in double-blind, randomized and parallel design with 23 subjects assigned to low-dose (40mg/dose, 80mg/ day) SP-8203 group, high-dose (80mg/dose, 160mg/day) SP-8203 group or placebo group, respectively.

If a subject, who is able to be enrolled in Stage 2, has neurological deficit of ≥4 point on NIHSS score and give patient's consent to participate in the trial, randomization will be performed and each treatment arm (one of three) will be assigned. The subject will receive the Investigational products a total of 6 times, with 12 hours intervals. Blood sample will be taken after the sixth administration of the Investigational product for pharmacokinetic and pharmacodynamics analysis. For pharmacokinetic analysis , blood sample will be taken at 0, 30, and 120 minutes after the complete sixth administration of the investigational products. For pharmacodynamics analysis, blood sample will be taken at between 24 to 48 hours after the first administration, at 0 minute after the sixth administration and at 4th week visit.

As with Stage 1, the subject will have brain MRI and MRA performed after the administration of investigational product, and brain CT will be performed at 24 hours after completion of the first administration of investigational products.

Brain MRI and MRA will be followed-up on Day 5, similarly to Stage 1. However, in Stage 2, the subject will make a visit for close monitoring for patient's neurological condition at 4th week and 12th week. Thereafter, all the procedures of the clinical trial will be completed.

Study Type

Interventional

Enrollment (Actual)

80

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Korea, Republic of
      • Busan, Korea, Republic of
        • Pusan National University Hospital
      • Daegu, Korea, Republic of
        • Kyungpook National University Hospital
      • Gyeonggi-do, Korea, Republic of
        • Myongji Hospital
      • Pusan, Korea, Republic of
        • Inje University Busan Paik Hospital
      • Seoul, Korea, Republic of
        • Kyunghee University Medical Center
      • Seoul, Korea, Republic of
        • Korea University Guro Hospital
      • Seoul, Korea, Republic of
        • Soonchunhyang University Hospital
      • Seoul, Korea, Republic of
        • Asan Medical Center, University of Ulsan

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

19 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Stage 1-specific Criteria Patients with neurologic deficit of ≥4 points and ≤10 points by NIHSS score.

Stage 2-specific Criteria Patients with neurologic deficit of ≥4 points by NIHSS score.

Common Criteria for Stage 1 and Stage 2

  1. Adults aged ≥19 years and ≤80 years.

  2. Subjects fulfilling the criteria for rtPA therapy. ① Subjects who can receive rtPA therapy within 4.5 hours after the onset of early symptoms of acute ischemic stroke.

    ② Subjects requiring rtPA therapy according to the judgment of a neurologist.

  3. Subjects available for brain MRI (DWI, GRE/SWI [Susceptibility Weighted Imaging], FLAIR, MRA) scanning
  4. Subjects who consent to participate in this trial.

Exclusion Criteria:

  1. Patients with systemic allergic diseases or hypersensitivity to specific drugs.
  2. Patients have condition as follows:
  1. Patients who were diagnosed with acute myocardial infarction (AMI) within the last 6 months.
  2. Patients who had arrhythmia causing symptoms such as dyspnea or palpitation within the last 6 months.

  3. Patients showing the following abnormal ECG findings in stable condition at screening:

    • The range of pulse rate - below 60/min or above 120/min

      • 2nd or 3rd degree AV(Atrioventricular) block indicated in ECG

        • Congenital or acquired QT syndrome indicated in ECG

          ④ Pre-excitation syndrome indicated in ECG

          3) Patients with severe heart failure of NYHA(New York Heart Association) Class III or Class IV.

NYHA classification of heart failure defined as:

Class I: patients with no limitation of activities; they suffer no symptoms from ordinary activities.

Class II: patients with slight, mild limitation of activity; they are comfortable with rest or with mild exertion.

Class III: patients with marked limitation of activity; they are comfortable only at rest.

Class IV: patients who should be at complete rest, confined to bed or chair; any physical activity brings on.

4) Patients with fever (≥ 38℃) or infection signs which require antibiotics at screening 5) Patients with pulmonary diseases (asthma, COPD[Chronic Obstructive Pulmonary Disease ], and active tuberculosis etc.) who have being recently been treated more than 1 month at screening, 6) Patients showing the following hematological findings: Patients with decreased hemoglobin (Hb< 10g/dL), decreased platelet count (PLT< 100,000/mm3) or hematocrit of <25% in complete blood count .

7) Patients who have undergone hemodialysis and/or treatments due to nephropathies, acute or chronic renal failure at screening.

8) Patients with a cancer in following conditions: diagnosed within 6 months before the screening time, or any treatment for cancer within the previous 6 months, or with recurrent/ metastatic cancer 9) Pregnant and breast-feeding women. However, women of childbearing age can participate in the trial only when non-pregnancy is confirmed. Woman of childbearing age is defined as woman who is not definitely menopause and did not receive a surgical contraception 10) Patients who do not consent to use double barrier contraception during the trial period.

11) Patients who have participated in other clinical trials of other drugs within the past 3 months. However, if they participated in observational studies and did not take drugs, they can participate in this trial.

12) Patients who cannot participate in the trial according to the judgment of investigators.

13) Patients with contraindication for the use of rtPA as shown in the below. [Contraindication for the Use of rtPA] A. Patients with hypersensitivity to gentamycin

B. rtPA should not be administered when the risk of bleeding is high as follows:

i. Patients who suffered from significant hemorrhagic diseases within the past 6 months or with known hemorrhagic diathesis.

ii. Patients receiving oral anticoagulants such as warfarin sodium (INR>1.3). iii. Patients with apparent hemorrhage or recent serious or risky hemorrhage. iv. Patients with the past history of tumor, aneurysm, or central nervous system damage such as intracranial or intraspinal operation.

v. Patients with hemorrhagic retinopathy, diabetes accompanied with visual disturbance or other ophthalmic hemorrhage.

vi. Patients who underwent prolonged or traumatic cardiopulmonary resuscitation (>2 minutes), obstetrical delivery or recently incompressible vascular puncture within the recent 10 days.

vii. Patients with uncontrollable severe arterial hypertension. viii. Patients who have underwent major surgery for the recent 3 months or had recently significant trauma including all the trauma cases related with acute myocardial infarction or head trauma.

ix. Patients with bacterial endocarditis and pericarditis. x. Patients with acute pancreatitis. xi. Patients confirmed to have records of ulcerative gastrointestinal diseases, esophageal varix, aneurysm or arteriovenous malformation for the recent 3 months.

xii. Patients with severe liver diseases including hepatic failure, liver cirrhosis, portal hypertension (esophageal), or active hepatitis.

C. Patients with mild neurologic deficit of <4 points on the NIHSS, or severe condition of >25 points on the NIHSS.

D. Patients with seizure at onset of stroke. E. Patients with clinical presentation which suggests a subarachnoid hemorrhage, even if initial CT scan is normal.

F. Patients who received heparin and have elevated active partial thromboplastin time (aPTT) within 48 hours before the onset of stroke.

G. Patients who has history of stroke or had head injury within the recent 3 months.

H. Patients with systolic blood pressure of >185mmHg or diastolic BP of >110mmHg, or who require aggressive treatment (intravenous administration) to reduce BP to the limits.

I. Patients with blood glucose level of <50mg/dL or >400mg/dL.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: SP-8203 High dose group
SP-8203 160mg (80mg/dose twice a day for three days)
Drug: SP-8203 High dose
High-dose group: 160mg will be intravenously administered as 80mg/dose twice daily (intervals of 12 hours).
Other Names:
  • SP-8203 is produced by Shin Poong Pharmaceutical company
Experimental: SP-8203 Low dose group
SP-8203 80mg (40mg/dose twice a day for three days)
Drug: SP-8203 Low dose
Low dose group: 80mg will be intravenously administered as 40mg/dose twice daily (intervals of 12 hours).
Other Names:
  • SP-8203 is produced by Shin Poong Pharmaceutical company
Placebo Comparator: Placebo group
Placebo group: twice a day for three days
Drug: Placebo
Same dosage of SP8203. Placebo will be intravenously administered twice daily (intervals of 12 hours)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The ratio of the incidence of parenchymal hematoma observed on brain CT
Time Frame: Brain CT should be performed at 24 ± 3 hours after the complete administration of the first dose of IP. (Screening, Baseline ,Day 0, Day 1)
Incidence of parenchymal hematoma observed on brain CT performed at 24 hours in accordance with European Cooperative Acute Stroke Study (ECASS) I and II criteria
Brain CT should be performed at 24 ± 3 hours after the complete administration of the first dose of IP. (Screening, Baseline ,Day 0, Day 1)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence rate of serious adverse events
Time Frame: Follow up period is 30 days after the last visit.
Incidence rate of serious adverse events
Follow up period is 30 days after the last visit.
Neurologic outcomes evaluated by modified Rankin Scale (mRS)
Time Frame: Screening, Baseline, Day 0, Day 5, Week 12, Early Termination
Neurologic outcomes evaluated by modified Rankin Scale (mRS)
Screening, Baseline, Day 0, Day 5, Week 12, Early Termination
Incidence rate symptomatic intracranial hemorrhage (sICH) occuring within 5 days
Time Frame: Day 1 Brain CT, Day 5 Brain MRI
Incidence rate symptomatic intracranial hemorrhage (sICH) occuring within 5 days
Day 1 Brain CT, Day 5 Brain MRI
Neurologic outcomes evaluated by NIHSS
Time Frame: NIHSS should be scored every visit
Neurologic outcomes evaluated by NIHSS
NIHSS should be scored every visit
Neurologic outcomes evaluated by Barthel Index
Time Frame: Day 0, Day 5, Week 12, Early Termination
Neurologic outcomes evaluated by Barthel Index
Day 0, Day 5, Week 12, Early Termination
The rate of death due to any cause
Time Frame: it is expected that a follow-up for up to 30 days after the last visit.
The rate of death due to any cause
it is expected that a follow-up for up to 30 days after the last visit.
Incidence rate of adverse events and adverse drug reactions
Time Frame: it is expected that a follow-up for up to 30 days after the last visit.
Incidence rate of adverse events and adverse drug reactions
it is expected that a follow-up for up to 30 days after the last visit.
Incidence rate of major systemic bleeding according to the International Society on Thrombosis and Hemostasis (ISTH
Time Frame: Laboratory tests (hematological test, clinical chemistry test, urinalysis etc.)- Day 1, Day 3, Day-5, Week 4, Week 12
Incidence rate of major systemic bleeding according to the International Society on Thrombosis and Hemostasis (ISTH
Laboratory tests (hematological test, clinical chemistry test, urinalysis etc.)- Day 1, Day 3, Day-5, Week 4, Week 12

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Shin Poong Pharmaceutical Co. Ltd.

Investigators

  • Principal Investigator: Jong Sung Kim, MD, Phd, Department of Neurology, Asan Medical Center, Seoul, South Korea

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 5, 2016

Primary Completion (Actual)

May 30, 2017

Study Completion (Actual)

August 22, 2017

Study Registration Dates

First Submitted

May 18, 2016

First Submitted That Met QC Criteria

May 25, 2016

First Posted (Estimate)

June 1, 2016

Study Record Updates

Last Update Posted (Actual)

July 21, 2020

Last Update Submitted That Met QC Criteria

July 20, 2020

Last Verified

July 1, 2020

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • SP-8203-2001

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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