Remove clinical dry-eye-disease
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US FDA approves Bausch + Lomb and Novaliq’s DED treatment Miebo

Pharmaceutical Technology

The US Food and Drug Administration (FDA) has granted approval to Bausch + Lomb and Novaliq’s Miebo (perfluorohexyloctane ophthalmic solution) to treat the signs and symptoms of dry eye disease (DED). It is the first and only prescription eye drop to receive FDA approval to treat DED that targets tear evaporation directly.

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Senju Pharmaceutical and Novaliq close agreement for dry eye disease therapy

Pharmaceutical Technology

Senju Pharmaceutical and Novaliq have closed a licence agreement for NOV03 (perfluorohexyloctane ophthalmic solution) to treat dry eye disease in Japan. Senju Pharmaceutical president Shuhei Yoshida stated: “We are thrilled to collaborate with Novaliq as a pioneer for cutting-edge water-free eye drop technology. “On

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FDA accepts Aldeyra Therapeutics’ NDA for dry eye disease therapy

Pharmaceutical Technology

The US Food and Drug Administration (FDA) has accepted Aldeyra Therapeutics’ new drug application (NDA) for topical ocular reproxalap to treat signs and symptoms of dry eye disease. It also includes evaluation in dry eye chamber challenge and natural environment settings, crossover and parallel-group study designs.

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Industry Briefs April 2023

PM360

Grifols and Selagine Tackle Dry Eyes The two eyecare leaders have entered a research, development, and sublicense agreement to develop and commercialize immunoglobulin eye drops for dry eye disease. Selagine, Inc. , Selagine, Inc. ,

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Alcon eyes $770m takeover of ophthalmology specialist Aerie

pharmaphorum

If completed, the deal will add two commercial products to Alcon’s range – glaucoma therapies Rocklatan (netarsudil/latanoprost) and Rhopressa (netarsudil) – as well as a pipeline of clinical and preclinical drug candidates currently headed by AR-15512, in phase 3 for dry eye disease.

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Théa Open Innovation signs licence deal with Galimedix

Pharmaceutical Technology

Under the agreement’s terms, TOI will receive exclusive rights to develop and commercialise Galimedix Therapeutics’ disease-modifying compound, GAL-101. It is currently ready to enter Phase II/III clinical trials. GAL-101 binds to a specific motif from Aβ that is exposed only in the misfolded Aβ monomer form and can be targeted.

Sales 52
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EC approves lebrikizumab for atopic dermatitis

European Pharmaceutical Review

ADvocate 1 and ADvocate 2, which evaluated lebrikizumab as monotherapy, demonstrated early clinical efficacy at week 16, reducing disease extent and severity by at least 75 percent in almost six out of 10 patients. Common reactions included conjunctivitis, injection site reactions, allergic conjunctivitis, and dry eye.

Safety 84