patients with elevate intraocular pressure MedDRA version: 18.0 Level: HLGT Classification code 10018307 Term: Glaucoma and ocular hypertension System Organ Class: 10015919 - Eye disorders
Conditions
Interventions
ALB 7208
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 2-
Pharmaceutical form of the placebo: Tablet
Route of administration of the placebo: Oral use
Sponsors
Can-Fite BioPharma Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Male or female, 18 years of age and over; 2. Ocular hypertension or open-angle glaucoma in at least 1 eye, diagnosed as any of the following: a. Untreated ocular hypertension without glaucomatous anatomic or VF changes; or b. Glaucoma diagnosed within the past 2 months but untreated; c. Previously treated glaucoma, provided that previous medication treatment has been inefficacious and/or intolerable, and has therefore been discontinued at least 3 weeks prior to Baseline; or d. Currently treated glaucoma with inadequate IOP control, meaning that IOP remains above target pressure as judged by the Investigator despite =3 weeks of treatment with a standard topical regimen (for guidance, the European Glaucoma Society defines “target pressure” as follows: “In most cases a peak IOP = 8 mm – 15 mmHg on a diurnal curve, or 30% IOP reduction from baseline”); 3. In subjects receiving a standard topical treatment regimen (per 2.d. above), the regimen and dose have not changed within 3 weeks of Screening, and are expected to remain stable throughout the treatment period; 4. At both Screening and Baseline, IOP in at least 1 eye (“candidate” eye) is >21 mmHg at 0800-1000 hours and >21 mmHg in at least 1 measurement at least 3 hours following the first (see Section 8.2.2); 5. Corneal thickness between 500 and 580 microns in both eyes (see Section 8.2.2); 6. Corrected visual acuity +0.18 logMAR or better by Early Treatment Diabetic Retinopathy Study (ETDRS) methodology in the candidate eye (equivalent to 20/30); 7. Females of child-bearing potential must have a negative blood pregnancy test at screening and throughout the study, to be eligible for, and continue participation in, the study; 8. Females of child-bearing potential must be willing to use 2 methods of contraception deemed adequate by the Investigator (eg, oral contraceptive pills plus a barrier method) to be eligible for, and continue participation in, the study; 9. Ability to complete the study in compliance with the protocol; and 10. Ability to understand and provide written informed consent. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 15 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 5
Exclusion criteria
Exclusion criteria: 1. IOP >32 mmHg in either eye; 2. History of angle-closure glaucoma; 3. Anatomically narrow angles in either eye (ie, =75% of the circumference of the angle must be =Grade 2 by Shaffer criteria2); 4. In subjects with glaucoma, advanced VF defect in either eye, determined on reliable testing using the Humphrey Full- Threshold Algorithm for the Glaucoma Hemifield Test (see Section 8.2.2), defined as either: a. Mean deviation worse than -16 dB, or b. Threat to fixation (sensitivity 10 dB or worse affecting either or both test points closest to the point of fixation in the upper hemifield and at either or both the corresponding test points in the lower hemifield); 5. In subjects with ocular hypertension, a score of >12 points on The Ocular Hypertension Treatment Study Group and European Glaucoma Prevention Study Group Primary Open- Angle Glaucoma Risk Table (see Appendix 2 in Section 17); 6. Documented disc hemorrhage within the past 5 years in either eye; 7. Secondary cause of IOP elevation; 8. Glaucoma laser treatment in candidate eye within the past 3 months; 9. Clinically significant ocular trauma to candidate eye within the past 6 months; 10. Any major ocular surgery in the past, including keratorefractive surgery, in candidate eye, except for uncomplicated cataract surgery performed greater than 6 months prior to Screening; 11. Astigmatism >3 diopters in either eye; 12. Clinically significant acute or chronic ocular disease (eg, corneal edema, uveitis, severe keratoconjunctivitis sicca, active ocular infection, active herpes simplex keratitis, blepharitis, or acute conjunctivitis) that might interfere with the study; 13. Concomitant contact lens use; 14. Concomitant use of systemic medication that may affect IOP (eg, beta blockers, corticosteroids, calcium channel blockers, ACE inhibitors, or carbonic anhydrase inhibitors); however, systemic antihypertensive medications are allowed providing that the dose and regimen have been stable for at least 3 months prior to Screening and are expected to remain stable throughout the trial; 15. Any abnormality preventing reliable applanation tonometry; 16. Presence of uncontrolled asthma; 17. Presence of uncontrolled arterial hypertension or symptomatic hypotension; 18. Significant cardiac arrhythmia or conduction block, congestive heart failure (New York Heart Association Class 3-4), or any other evidence of clinically significant heart disease or clinically significant findings on screening ECG; 19. Hemoglobin level <9.0 gm/L at screening; 20. Platelet count <125,000/mm3 at screening; 21. White blood cell count <3500/mm3 at screening; 22. Serum creatinine level greater than 1.5 times the laboratory’s upper limit of normal (ULN) at screening; 23. Liver aminotransferase levels greater than 2 times the laboratory’s ULN at screening; 24. Known or suspected immunodeficiency or human immunodeficiency virus positivity; 25. Known infection with hepatitis B or C; 26. Pregnancy, planned pregnancy, lactation, or inadequate contraception as judged by the Investigator; 27. Previous receipt of CF101; 28. History of malignancy within the past 5 years (excluding basal cell carcinoma of the skin and =3 cutaneous squamous cell carcinomas, all of which have been completely excised); 29. Active drug or alcohol dependence; 30. Significant acute or chronic medical, ophthalmic, neurologic, or psychiatric illness that, in the judgment of the Investig
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: Determine the effects of oral CF101 in lowering intraocular pressure (IOP) when administered twice daily for 16 weeks in subjects with elevated IOP; and Determine the safety of oral CF101 in this subject population ;Secondary Objective: Not applicable;Primary end point(s): Efficacy: Effects on IOP; Safety: AE reporting, physical examination, vital signs, ophthalmologic and slit lamp examination, (VF) assessments, clinical laboratory testing ;Timepoint(s) of evaluation of this end point: 2 - 16 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary end point(s): Not applicable;Timepoint(s) of evaluation of this end point: Not applicable | — |
Countries
Bulgaria, India, Israel
Contacts
Public ContactMedical Director
Can-Fite BioPharma Ltd.
Outcome results
None listed