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On average, our surveys take only 5 to 15 minutes to complete. Survey results help you analyze practice patterns, evaluate treatment choices, and benchmark your practice.

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Latest Market Reports

Market Scope's industry reports are meticulously prepared by a dedicated team of in-house consultants/analysts with over 100 years of collective experience.

Latest Industry News & Trends

10/11/2018
orthopedicpress release
Market Scope Announces Launch of New Website and Entry into Orthopedics

Market Scope, an industry leader for ophthalmic market research, announced today the launch of its new website and the firm’s entry into orthopedics, its second medical vertical. The new Market-Sco...

1/18/2019
breakingophthalmic
US FDA Accepts IND Application for Aerie’s AR-1105, a Dexamethasone Intravitreal Implant

The US FDA has approved Aerie Pharmaceuticals’ investigational new drug (IND) Application for AR-1105 (dexamethasone intravitreal implant) for macular edema due to retinal vein occlusion (RVO), the...

1/18/2019
breakingophthalmic
Glaukos Moving to Aliso Viejo from San Clemente

Glaukos will move its headquarters in May to Aliso Viejo, California, from San Clemente, California, according to an SEC filing. The company will lease three existing office buildings in Aliso Viej...

1/18/2019
breakingophthalmic
Ocular Therapeutix Seeks to Expand Dextenza’s Indication

Ocular Therapeutix has submitted a supplemental new drug application (sNDA) to the US FDA for Dextenza, the Bedford, Massachusetts, company announced Jan. 10. The sNDA seeks to expand the product’s...

1/18/2019
breakingophthalmic
Aerpio Completes Patient Dosing in Phase IIb Study for Diabetic Retinopathy Candidate

Aerpio Pharmaceuticals has completed patient dosing in its Phase IIb clinical trial of AKB-9778 for severe nonproliferative diabetic retinopathy (NPDR), the Cincinnati company announced Jan. 17. AK...

1/18/2019
breakingophthalmic
FDA Accepts Xbrane’s Application to Begin Study of Xlucane, a Biosimilar of Lucentis

Xbrane reported Jan. 18 that the US FDA accepted the company’s application for a pivotal Phase III trial of Xlucane as a biosimilar to Lucentis in patients with wet age-related macular degeneration...

1/18/2019
breakingophthalmic
Akorn Receives US FDA Warning Letter Citing Plant Violations

Akorn has received a warning letter from the US FDA after an inspection of its Decatur, Illinois, manufacturing plant, the Lake Forest, Illinois, company announced Jan. 9. The warning letter lists ...

1/18/2019
newsletterorthopedic
Flexion Announces Positive Results for Phase II Trial of Zilretta

Massachusetts-based Flexion Therapeutics announced Jan. 2 that its Phase II pharmacokinetic study of Zilretta for OA of the shoulder and hip achieved positive results. Zilretta is the only extended...

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