Safety and Efficacy Study of CF101 to Treat Keratoconjunctivitis Sicca

Keratoconjunctivitis Sicca Clinical Trial

Official title:

A Phase 2, Randomized, Double-Masked, Placebo-Controlled, Parallel-Group Study of the Safety and Efficacy of Daily CF101 Administered Orally in Patients With Moderate-to-Severe Keratoconjunctivitis Sicca

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00349466
• Other study ID #: CF101-201KCS
• Status: Completed
• Phase: Phase 2
• Start date: January 2007
• Est. completion date: May 2009

Study information

• Verified date: February 2022
• Source: Can-Fite BioPharma
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase 2, randomized, double-masked, placebo-controlled, parallel-group study in adult males and females, aged 18 years and over, with a diagnosis of moderate-to-severe keratoconjunctivitis sicca (KCS). Patients will be randomized to receive either CF101 1 mg or matching placebo, given orally every 12 hours (q12h) for 12 weeks. A Screening Period of up to 4 weeks that includes a 2-week run-in period will precede a 12-week treatment period, followed by a 2-week follow-up period.

Description:

At a Screening Visit, patients who provide written informed consent will have screening procedures performed, including a complete medical history, medication history, physical examination, including height, weight, sitting blood pressure, pulse rate and temperature, and clinical laboratory tests. Disease activity will be assessed using tear meniscus (TM) height, tear break-up time (BUT), fluorescein staining (FS), Schirmer test, and the Dry Eye Symptom Score (DESS). Doses of artificial tears must be stable for >2 weeks prior to the Screening Visit.

Eligible patients will begin a 2-week run-in period, during which time they will be instructed to discontinue use of all topical ophthalmic medications except for lubricant eye drops. Patients who successfully complete the 2-week run-in period will be randomized to their assigned medication (CF101 1 mg or matching placebo) to be taken orally every q12h for 12 weeks. Patients will return for assessments and a new supply of study medication at Weeks 2, 4, 8 and 12, and at Week 14 for a final follow-up assessment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: May 2009
• Est. primary completion date: May 2009
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female, 18 years of age and over;

• Have a diagnosis of moderate-to-severe KCS as defined by: (1) Schirmer Test (ST) (without anesthesia) < 7 mm/5 min in either eye; AND (2) Positive FS, defined as a corneal punctate fluorescein staining score of =1 in either eye, where 0 = none and 3= severe; AND (3) At least 1 of the following ocular symptoms scored at =2, where 0 = none and 4 = very severe/interferes with normal activities: photophobia, blurred vision, foreign body sensation, soreness or pain, itching, burning, dryness;

• Willing to use no topical ocular treatments except for the unpreserved artificial tears;

• Doses of unpreserved artificial tears have been stable for >2 weeks prior to Screening Visit;

• 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;

• Females of child-bearing potential must be willing to use 2 methods of contraception deemed adequate by the Investigator (for example oral contraceptive pills plus a barrier method) to be eligible for, and continue participation in, the study;

• Ability to complete the study in compliance with the protocol; and

• Ability to understand and provide written informed consent.

Exclusion Criteria:

• Has Sjögren's Syndrome with significant systemic non-exocrine gland involvement;

• Has Stevens-Johnson Syndrome;

• If KCS is due to rheumatoid arthritis or other autoimmune diseases, patient may not be receiving disease-modifying drugs, including methotrexate and biological agents;

• Use of systemic immunosuppressive drugs;

• Use of oral corticosteroids >10 mg prednisone, or equivalent, per day;

• Use of topical steroids within 2 weeks prior to the Screening Visit and for the duration of the study;

• Receipt of topical cyclosporine eye drops within 3 months prior to the Screening Visit and for the duration of the trial;

• Presence of chronic ocular disease other than KCS requiring topical treatment;

• Presence of post-burn ocular injury;

• Ocular herpes simplex virus infection;

• Concomitant use of contact lenses;

• Persistent intraocular inflammation or infection;

• Active blepharitis;

• Recent surgical occlusion of the lacrimal puncta;

• Subepithelial corneal scarring;

• Anesthetic or neurotrophic corneas;

• Hemoglobin level <9.0 gm/L;

• Platelet count <125,000/mm^3;

• White blood cell count <3500/mm^3;

• Serum creatinine level outside the laboratory's normal limits;

• Liver aminotransferase levels greater than 2 times the laboratory's upper limit of normal;

• Pregnancy, planned pregnancy, lactation, or inadequate contraception as judged by the Investigator;

• History of malignancy within the past 5 years (excluding basal cell carcinoma of the skin);

• Significant acute or chronic medical, ophthalmic, or psychiatric illness that, in the judgment of the Investigator, could compromise patient safety, limit the patient's ability to complete the study, and/or compromise the objectives of the study;

• Participation in another investigational drug or vaccine trial concurrently or within 30 days; or

• Other conditions which would confound the study evaluations or endanger the safety of the patient.

Related Conditions & MeSH terms

• Dry Eye Syndromes
• Keratoconjunctivitis
• Keratoconjunctivitis Sicca

Intervention

Drug:
• CF101
Orally CF101 1mg
• Placebo
Orally matching Placebo

Locations

Country	Name	City	State
Israel	Meir Hospital	Kfar-Saba
Israel	Sheba Medical Center	Tel Hashomer
Israel	Assaf Harofeh Medical Center	Tsrifin

Sponsors (1)

Lead Sponsor	Collaborator
Can-Fite BioPharma

Country where clinical trial is conducted

Israel, 

References & Publications (1)

Avni I, Garzozi HJ, Barequet IS, Segev F, Varssano D, Sartani G, Chetrit N, Bakshi E, Zadok D, Tomkins O, Litvin G, Jacobson KA, Fishman S, Harpaz Z, Farbstein M, Yehuda SB, Silverman MH, Kerns WD, Bristol DR, Cohn I, Fishman P. Treatment of dry eye syndr — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change From Baseline to Week 12 in Schirmer Test (ST) Score in Millimeters	Involved placing a standardized paper tear strip inside the lower eyelid for 5 minutes. The tear strip was then removed and the length of the strip that was wet from tears was measured in millimeters. Change from baseline is calculated. Scores range 0-35 mm, with higher scores indicating more (better) tear production.	12 weeks
Primary	Change From Baseline to Week 12 in Tear Break-Up Time (BUT) in Seconds	Time elapsed between a complete blink and the development of the first random dry spot on the tear film as seen under fluorescent light. Change from baseline is calculated. Scores range 0-30 seconds, with higher scores indicating better tear composition and function.	12 weeks
Primary	Number of Subjects With >25% Improvement in Fluorescein Staining of the Cornea (FS) at Week 12	Severity of corneal epithelial loss as graded by Fluorescein Staining of the cornea, assessed on a 0-4+ scale with 0 = none and 4+ = severe de-epithelialization (in other words, higher scores indicate worse disease), expressed as number of participants with >25% improvement at Week 12 relative to baseline.	12 weeks
Secondary	Number of Subjects Experiencing Clinical Success at Week 12	Proportion of subjects experiencing improvement of =25% over baseline at Week 12 in (a) tear breakup time (BUT), (b) superficial punctate keratitis as assessed by fluorescein staining (FS), or Schirmer Test (ST)	12 weeks
Secondary	Change From Baseline to 12 Weeks in Dry Eye Symptom Score (DESS)	DESS consists of 12 questions designed to assess the symptoms of ocular irritation, covering three areas: ocular symptoms, environmental triggers and vision-related function. Each of the 12 symptoms can be graded 0-4, with 0 indicating no symptoms over the past week, and 4 meaning constant symptoms over the past week. Scores from all answered questions are summed. The final score is multiplied by (25/number of questions answered) to give an outcome between 0 (no symptoms) to 100 (worst possible symptoms). Change from baseline is calculated.	12 weeks
Secondary	Change From Baseline to Week 12 in Tear Meniscus (TM) Height	Indicator of tear volume. TM was recorded on a scale from 0-3, with 0=none, 1=trace, 2=normal, and 3=high, with higher scores meaning better tear production and integrity. Change from baseline.	12 weeks
Secondary	Percent Change From Baseline to Week 12 in the Use of Artificial Tears	Daily use of REFRESH TEARS® Lubricant Eye Drops artificial tears supplied to each patient was recorded in diaries provided to patients. Percent change from baseline is calculated.	12 weeks

External Links

•   Can-Fite BioPharma web site