Latest News in the pharma Industry

Research & Development

BMS to sell its HIV R&D portfolio to ViiV Healthcare

BMS to sell its HIV R&D portfolio to ViiV Healthcare

18 Dec 2015

Transactions are consistent with the evolution of BMS’s strategic focus, including the decision to discontinue its discovery efforts in virology announced in June.

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Merck and Pfizer receive FDA Breakthrough Therapy Designation for avelumab in metastatic Merkel cell carcinoma

Merck and Pfizer receive FDA Breakthrough Therapy Designation for avelumab in metastatic Merkel cell carcinoma

18 Nov 2015

If approved, avelumab could potentially become the first immunotherapy to treat metastatic MCC.

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Lucentis effective for proliferative diabetic retinopathy

Lucentis effective for proliferative diabetic retinopathy

18 Nov 2015

NIH-funded clinical trial marks first major advance in therapy in 40 years.

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FLAME study shows superiority of Novartis' Ultibro Breezhaler over Seretide in reducing COPD exacerbations

FLAME study shows superiority of Novartis' Ultibro Breezhaler over Seretide in reducing COPD exacerbations

17 Nov 2015

First large-scale study to confirm Ultibro Breezhaler is an effective steroid-free option that both reduces exacerbations and improves lung function in COPD patients with one or more exacerbations in the past year, compared to Seretide.

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Concert Pharmaceuticals achieves $2 million milestone from Avanir Pharmaceuticals for Phase III Initiation of AVP-786 for agitation in patients with Alzheimer’s disease

Concert Pharmaceuticals achieves $2 million milestone from Avanir Pharmaceuticals for Phase III Initiation of AVP-786 for agitation in patients with Alzheimer’s disease

16 Nov 2015

The collaboration agreement between Concert and Avanir provides Avanir with worldwide rights to develop and commercialize AVP-786 and other deuterium-modified dextromethorphan (d-DM) compounds.

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Positive Phase I/II interim data of Bimatoprost sustained-release implant for IOP therapy in glaucoma

Positive Phase I/II interim data of Bimatoprost sustained-release implant for IOP therapy in glaucoma

16 Nov 2015

Bimatoprost SR is a biodegradable, intracameral implant providing slow release of bimatoprost and is a differentiated approach to treat glaucoma beyond conventional daily eye drop treatments because it is a non-daily treatment administered by a physici...

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Allergan presents data at the 2015 American Academy of Ophthalmology Annual Meeting in Las Vegas

Allergan presents data at the 2015 American Academy of Ophthalmology Annual Meeting in Las Vegas

13 Nov 2015

Five oral presentations include “Long-Term Response to Anti-VEGF Therapy for DME Can be Predicted After 3 Injections — An Analysis of Protocol I Data”.

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FDA approves Roche’s Cotellic in combination with Zelboraf in advanced melanoma

FDA approves Roche’s Cotellic in combination with Zelboraf in advanced melanoma

12 Nov 2015

FDA approval underscores the important role of targeted medicines to help people with BRAF V600 mutation-positive advanced melanoma.

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Concert Pharmaceuticals initiates Phase I multiple ascending dose trial with CTP-656 for cystic fibrosis

Concert Pharmaceuticals initiates Phase I multiple ascending dose trial with CTP-656 for cystic fibrosis

12 Nov 2015

A novel, potentially disease-modifying treatment for cystic fibrosis for use as monotherapy as well as in combination with other CFTR modulators.

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Amgen presents detailed results from Phase III study demonstrating clinical equivalence of biosimilar candidate ABP 501 with adalimumab

Amgen presents detailed results from Phase III study demonstrating clinical equivalence of biosimilar candidate ABP 501 with adalimumab

12 Nov 2015

First completed Phase III study of adalimumab biosimilar in the treatment of patients with moderate-to-severe RA.

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Regeneron and Sanofi announce new Praluent injection analyses presented at AHA scientific sessions 2015

Regeneron and Sanofi announce new Praluent injection analyses presented at AHA scientific sessions 2015

11 Nov 2015

74% of patients reached their LDL cholesterol goals on 75 mg dose; Of the remaining patients whose dose was adjusted to 150 mg, most achieved their goal.

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Teva granted Breakthrough Therapy Designation for SD-809 by FDA

Teva granted Breakthrough Therapy Designation for SD-809 by FDA

9 Nov 2015

SD-809 — a much-needed treatment option for the tardive dyskinesia patient population.

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