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FST-100 in the Treatment of Acute Adenoviral Conjunctivitis

This study has been completed.
Information provided by (Responsible Party):
Shire Identifier:
First received: November 9, 2011
Last updated: September 22, 2015
Last verified: August 2014
This randomized, double masked, multi-center study is being conducted to support the safety and efficacy of FST-100 for the treatment of acute adenoviral conjunctivitis.

Condition Intervention Phase
Acute Adenoviral Conjunctivitis Drug: FST-100 Drug: FST-100 (Component #1) Drug: FST-100 Vehicle Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Proof-of-Concept, Multi-center, Randomized, Double-Masked Study to Evaluate the Clinical Efficacy and Safety of FST-100 Ophthalmic Suspension in the Treatment of Acute Adenoviral Conjunctivitis

Resource links provided by NLM:

Further study details as provided by Shire:

Primary Outcome Measures:
  • Adenoviral eradication and clinical resolution of the infection [ Time Frame: 6-7 days ]

Enrollment: 176
Study Start Date: December 2012
Study Completion Date: May 2014
Primary Completion Date: May 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: FST-100 Drug: FST-100
Experimental: FST-100 (Component #1) Drug: FST-100 (Component #1)
FST-100 (Component #1)
Placebo Comparator: FST-100 Vehicle Drug: FST-100 Vehicle
FST-100 Vehicle


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Have a clinical diagnosis of suspected acute adenoviral conjunctivitis in at least one eye.

Exclusion Criteria:

  • Have a known sensitivity to any of the components of FST-100 or FST-100 vehicle.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01470664

United States, Massachusetts
Ora, Inc.
Andover, Massachusetts, United States, 01810
Ora, Inc.
Noida, India, 201301
Sponsors and Collaborators
Study Director: Aron Shapiro ORA, Inc.
  More Information

Responsible Party: Shire Identifier: NCT01470664     History of Changes
Other Study ID Numbers: FST100-AVC-004
Study First Received: November 9, 2011
Last Updated: September 22, 2015

Additional relevant MeSH terms:
Conjunctivitis, Inclusion
Conjunctival Diseases
Eye Diseases
Conjunctivitis, Bacterial
Eye Infections, Bacterial
Bacterial Infections
Chlamydia Infections
Chlamydiaceae Infections
Gram-Negative Bacterial Infections
Eye Infections
Infection processed this record on September 21, 2017