P52901: Phase I Study of Palomid 529 a Dual TORC1/2 Inhibitor of the PI3K/Akt/mTOR Pathway for Advanced Neovascular Age-Related Macular Degeneration

• Sponsor: Paloma Pharmaceuticals, Inc. (Industry)
• Overall Status: Completed
• CT.gov ID: NCT01033721
• Collaborator: (none)
• Enrollment: 13
• Location: 1
• Duration (Months): 18
• Patients Per Site Per Month: 0.7

Study Details

Study Description

Brief Summary

Palomid 529 is a dual TORC1/2 inhibitor of the PI3K/Akt/mTOR pathway having broad activity in angiogenesis and cellular proliferation. Palomid 529 will be examined to determine if the safety, tolerability and pharmacokinetic profile of single ascending doses when administered intravitreally or subconjunctivally.

Condition or Disease	Intervention/Treatment	Phase
Age-Related Macular Degeneration	Drug: Palomid 529	Phase 1

Study Design

• Study Type: Interventional
• Actual Enrollment: 13 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: A Phase I Open-Label Study to Investigate the Safety, Tolerability and Pharmacokinetic Profile of Single Intravitreal and Subconjunctival Doses of Palomid 529 in Patients With Advanced Neovascular Age-Related Macular Degeneration (AMD)
• Study Start Date: Jun 1, 2010
• Actual Primary Completion Date: Dec 1, 2011
• Actual Study Completion Date: Dec 1, 2011

Outcome Measures

Primary Outcome Measures

1. Safety-Review AEs, concomitant meds-Vitals, HR, systolic/diastolic BP, temperature, weight-ECG changes; Physical exam-Laboratory parameters-Ophthalmic exam-visual acuity, IOP, slit lamp fundus exam, fundus photography, fluorescein angiography, OCT [43 days]

Secondary Outcome Measures

1. Efficacy-Mean change in visual acuity by ETDRS testing-Decreased leakage and/or size on FA, decreased retinal thickness in OCT-Decreased fibrosis if detectable based on fundus examination, photography, angiography and OCT [43 days]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 50 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Best corrected visual acuity in the study eye between 20/100 and 20/800 (between 53 and 4 ETDRS letters read), and better or equal to 20/200 (minimum of 34 letters read) in the fellow eye.

• Subfoveal choroidal neovascularization (CNV) due to AMD

• Total area of the lesion (including blood, neovascularization and scar/atrophy) must be < 12 DA.

• Only 1 eye will be treated in the study. If both eyes are eligible, the investigator will select the eye with the most active CNV

• Clear ocular media and adequate pupillary dilatation to permit good stereo fundus photography for screening

• Intraocular pressure of 21 mm Hg or less

• Retinal thickness ≥ 250 μm by OCT, with presence of intraretinal or subretinal fluid

Exclusion Criteria:

• Any retinovascular disease or retinal degeneration other than AMD

• Serous pigment epithelial detachment without the presence of neovascularization

• Previous posterior vitrectomy or retinal surgery

• Any periocular infection in the past 4 weeks

• Concomitant therapy with anti-VEGF therapies, e.g. Avastin, Lucentis or Macugen, or previous use of these agents within 60 days of screening

• Concomitant therapy with intravenous or intravitreous corticosteroids or use within 90 days of screening

• Significant media opacities, including cataract, which might interfere with visual acuity, assessment of toxicity, or fundus photography

• Cataract surgery in the study eye within 3 months of screening

• Intraocular surgery in the study eye within 3 months of screening

• Presence of ocular infection in the study eye

• Presence of severe myopia (-8 diopters or greater) in the study eye

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Ophthalmic Consultants of Boston	Boston	Massachusetts	United States	02114

Sponsors and Collaborators

• Paloma Pharmaceuticals, Inc.

Investigators

• Principal Investigator: Jeffrey S. Heier, M.D., Ophthalmic Consultants of Boston

Study Documents (Full-Text)

None provided.

More Information

Publications

• Lewis GP, Chapin EA, Byun J, Luna G, Sherris D, Fisher SK. Muller cell reactivity and photoreceptor cell death are reduced after experimental retinal detachment using an inhibitor of the Akt/mTOR pathway. Invest Ophthalmol Vis Sci. 2009 Sep;50(9):4429-35. doi: 10.1167/iovs.09-3445. Epub 2009 Apr 15.

• ClinicalTrials.gov Identifier: NCT01033721
• Other Study ID Numbers: Paloma P529 Ocular
• First Posted: Dec 16, 2009
• Last Update Posted: Sep 24, 2012
• Last Verified: Sep 1, 2012

• Additional relevant MeSH terms: Macular Degeneration

Study Results

No Results Posted as of Sep 24, 2012