| Eligibility |
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:
1. Untreated ocular hypertension without glaucomatous anatomic or VF changes; or
2. Glaucoma diagnosed within the past 2 months but untreated;
3. 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
4. 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;
5. Corneal thickness between 500 and 580 microns in both eyes;
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 urine 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.
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 criteria );
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,
defined as either:
1. Mean deviation worse than -16 dB, or
2. 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;
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 Investigator, could compromise subject safety, limit the
subject's ability to complete the study, and/or compromise the objectives of the
study;
31. Participation in another investigational drug or vaccine trial concurrently or within
30 days; or
32. Other conditions which would confound the study evaluations or endanger the safety of
the subject.
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