A Clinical Study of NTx®-265: human chorionic gonadotropin (hCG) and epoetin alfa (EPO) in acute ischemic stroke patients

Recruitment & Eligibility

Status: Open to Recruitment

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

1. Age 18-85.
2. NIHSS score 8-20 within 24-48 hours after stroke onset and enrolment.
3. Stroke is ischemic in origin, supratentorial, and radiologically confirmed (CT scan or diagnostic MRI) prior to enrolment.
4. Patient is 24-48 hours from time of stroke onset when the first dose of NTx®-265 therapy is administered. Time of onset is when symptoms began; for stroke that occurred during sleep, time of onset is when patient was last seen or was self-reported to be normal.
5. Reasonable expectation of availability to receive the full 9 day NTx®-265 course of therapy, and to be available for subsequent follow-up visits.
6. Reasonable expectation that patient will receive standard post-stroke physical, occupational, speech, and cognitive therapy as indicated.
7. Female patient is either :
a. not of childbearing potential, defined as postmenopausal for at least 1 year or surgically sterile (bilateral tubal ligation, bilateral oophorectomy or hysterectomy) or,
b. if of childbearing potential, agrees to use two of the following effective separate forms of contraception throughout the study, up to and including the follow up visits:
? condoms, sponge, foams, jellies, diaphragm or intrauterine device (IUD)contraceptives (e.g. implants, injectables, combined oral, etc.)
OR
? a vasectomized partner
OR
? abstinence

Exclusion Criteria

1. Patients presenting with lacunar, hemorrhagic and/or brain stem stroke
2. Patients who have received thrombolytic treatment with tPA following the index stroke
3. Patients classified as comatose, defined as a patient who requires repeated stimulation to attend, or is obtunded and requires strong or painful stimulation to make movements (NIHSS 1A score must be <2)
4. Women who have tested positive for pregnancy or are breast feeding or are not using a highly effective method of birth control that can be maintained for the duration of the study
5. Serum hemoglobin > 16 g/dL (males) or > 14 g/dL (females); or platelet count > 400,000/mm3
6. Advanced liver, kidney, cardiac or pulmonary disease; the former will be operationally defined using NCI Toxicity Criteria (Grade 2 or higher): Appendix I
7. Serum bilirubin > 1.5 x ULN
8. Alkaline phosphatase > 2.5 x ULN
9. AST or ALT > 2.5 x ULN
10. Creatinine > 2.0 x ULN
11. Patients with known and documented elevated PSA levels
12. Patients with a known history of hypercoagulability, including known cardiolipin / antiphospholipid antibody syndrome
13. Expected survival < 1 year
14. Allergy or other contraindication to hCG including:
a. Prior hypersensitivity to hCG preparations or one of their excipients
b. Primary ovarian failure
c. Uncontrolled thyroid or adrenal dysfunction
d. An uncontrolled organic intracranial lesion such as a pituitary tumor
e. Abnormal uterine bleeding of undetermined origin
f. Ovarian cyst or ovarian enlargement of undetermined origin
g. Sex hormone-dependent tumors of the reproductive organs, accessory sex glands, and breasts
15. Allergy or other contraindication to epoetin alfa:
a. Who developed pure red cell aplasia following treatment with any erythropoiesis regulating hormones
b. With uncontrolled hypertension
c. With known hypersensitivity to mammalian cell-derived products, albumin (human) or any component of the product
d. Who for any reason cannot receive adequate antithrombotic treatment
16. A known diagnosis of cancer in the previous 5 years (except non-malignant skin cancer)
17. Uncontrolled hypertension, defined in the context of acute stroke as blood pressure persistently above 220 mm Hg systolic or 120 mm Hg diastolic despite antihypertensive therapy
18. Use of either hCG or epoetin alfa within the previous 90 days
19. Any condition known to elevate hCG, active in the prior 24 months, e.g., choriocarcinoma or germ cell tumor
20. Patients with a pre-stroke/pre-morbid modified Rankin Score (mRS) ≥ 2
21. Any patients living in a nursing home or supervised living center. Patients must be historically fully independent in all activities of daily living including banking, shopping, cooking, toileting, showering and dressing.
22. Any other medical condition or degree of stroke such that, in the investigator?s opinion, the patient should not be included in the trial
23. With the exception of the qualifying stroke, any other stroke within the previous 3 months. Patients with asymptomatic stroke can be included if they meet the criteria described in Section 7.4.1.
24. Patients who cannot take anti-platelet or anti-coagulant therapy
25. Pre-existing and active major psychiatric or other chronic neurological disease
26. Consume, on average, greater than 14 alcoholic drinks per week, or have a history of substance abuse or dependency within 12 months prior to the study
27. Currently participating in another investigational study

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Modified Rankin Score (mRS)<br>NIHSS responseTimepoint: Day 90

Secondary Outcome Measures

Name	Time	Method
IHSS,<br>mRS,<br>Barthel Index,<br>Action Research Arm Test,<br>Gait Velocity Test,<br>Boston Naming Test,<br>Line cancellation test,<br>Trails A & B test,<br>Geriatric Depression Scale<br>Timepoint: Day 90

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