Treatment of Idiopathic Perifoveal Telangiectasia (IPT) With Open-Label Anecortave Acetate (15mg.).
Launched by MANHATTAN EYE, EAR & THROAT HOSPITAL · Sep 13, 2005
Trial Information
Current as of July 23, 2025
Completed
Keywords
ClinConnect Summary
In this open-label pilot study, an initial patient, which presented with IPT and SRN, was treated with promising success and five additional patients were then recruited. So this is a report on six eyes of the first six patients with this disease who presented in our practice. The Food and Drug Administration (FDA) granted our site permission to enroll these patients. While anecortave acetate has not yet been approved by the FDA, it has been used in phase 2/3 trials for the treatment of AMD. An informed consent was obtained from each patient. IRB approval was obtained from Manhattan Eye, Ea...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Clinical diagnosis of patients with Idiopathic Perifoveal Telangiectasia(IPT).
- • 2. Patients must be 18 years of age or older to receive treatment.
- • 3. Visual acuity of 20/30 to 20/320 Study Eye on the ETDRS visual acuity chart.
- • 4. Visual acuity of 20/800 or better Fellow Eye on the ETDRS visual acuity chart .
- Exclusion Criteria:
- • 1. Patient with significantly compromised visual acuity in the study eye due to concomitant ocular conditions.
- • 2. Patients who have undergone intraocular surgery within last 2 months.
- • 3. Patient participating in any other investigational drug study.
- • 3.Use of an investigational drug or treatment related or unrelated to their condition within 30 days prior to receipt of study medication.
- • 4.Inability to obtain photographs to document CNV (including difficulty with venous access).
- • 5.Patient with significant liver disease or uremia. 6.Patient with known adverse reaction to fluorescein and indocyanine green or iodine.
- • 7.Patient has a history of any medical condition which would preclude scheduled visits or completion of study.
- • 8.Patient has had insertion of scleral buckle in the study eye. 9.Patient has received radiation treatment 10.Patient is on anticoagulant therapy with the exception of aspirin 11.Patient is pregnant or nursing.
About Manhattan Eye, Ear & Throat Hospital
Manhattan Eye, Ear & Throat Hospital is a leading clinical research institution dedicated to advancing medical knowledge and treatment options in ophthalmology, otolaryngology, and related fields. With a commitment to patient-centered care and innovative research, the hospital collaborates with renowned specialists and utilizes state-of-the-art technology to conduct clinical trials aimed at improving health outcomes. Its focus on rigorous scientific methodology and ethical standards ensures the integrity and reliability of its research, contributing to the development of cutting-edge therapies and enhancing the overall quality of patient care.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
New York, New York, United States
Patients applied
Trial Officials
Lawrence A. Yannuzzi, MD
Principal Investigator
Manhattan Eye, Ear & Throat Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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