mtattory@lifescipublicrelations.com

/Michael Tattory

About Michael Tattory

This author has not yet filled in any details.
So far Michael Tattory has created 257 blog entries.

Overcome The Challenges Of An Ultra-Rare Disease Trial

ArQule is a personalized medicine company working in the oncology space to develop treatments that target specific mutations. The Massachusetts-based company faces many challenges in this space, including one that is common to many cancer treatments.

By | 2018-11-20T13:15:01-04:00 November 20th, 2018|News|Comments Off on Overcome The Challenges Of An Ultra-Rare Disease Trial

SQZ Biotech pushes forward with its method to squeeze drugs into cells

One Watertown, Mass.-based biotech is working to capitalize on growing momentum for cell and gene therapies — and it seems to have found its opening. The company is working on a technology that will squeeze cells to open up tiny pores in their membranes to deliver gene therapies or medicines straight into the cell. [...]

By | 2018-11-19T18:23:25-04:00 November 19th, 2018|News|Comments Off on SQZ Biotech pushes forward with its method to squeeze drugs into cells

Oxurion’s CEO Dr. Patrik De Haes discusses three pipeline candidates for diabetic eye disease

Patrik De Haes, MD, CEO of Oxurion, discusses the company’s three disease-modifying drug candidates for the treatment of diabetic eye disease with EyeWire News at the Ophthalmology Innovation Summit in Chicago.

By | 2018-11-20T09:59:09-04:00 November 19th, 2018|News, video|Comments Off on Oxurion’s CEO Dr. Patrik De Haes discusses three pipeline candidates for diabetic eye disease

Arena bags big deal with United for PAH drug ralinepag

Arena’s run of positive news continues, with a massive $800 million upfront licensing deal with United Therapeutics for its pulmonary arterial hypertension drug ralinepag. The global deal, which also includes $400 million in milestones and double-digit royalties, comes on the heels of well-regarded phase 2 data with the oral prostacyclin receptor agonist in PAH that caused [...]

By | 2018-11-19T18:21:22-04:00 November 15th, 2018|News|Comments Off on Arena bags big deal with United for PAH drug ralinepag

Could Pot Help Solve The Opioid Crisis?

A $238,000 federal study will follow more than 10,000 medical marijuana patients in New York over the next two years to see if their opioid use drops. Scott Jordan never thought weed would help him kick the painkillers he took for a bad back. “I smoked pot in high school,” he told BuzzFeed News. [...]

By | 2018-11-19T18:13:22-04:00 November 15th, 2018|News|Comments Off on Could Pot Help Solve The Opioid Crisis?

Arena Pharma soars on deal with United Therapeutics for hypertension drug

Shares of Arena Pharmaceuticals Inc jumped nearly 30 percent after the drug developer sold rights to develop and sell its hypertension treatment to United Therapeutics Corp, fetching it $800 million in an upfront payment. Arena Pharma said the money will help it prepare for the eventual launch of its bowel disorder drugs. [...]

By | 2018-11-19T14:26:32-04:00 November 15th, 2018|News|Comments Off on Arena Pharma soars on deal with United Therapeutics for hypertension drug

United Therapeutics pays $800M-plus to grab Arena’s PhIII PAH drug

United Therapeutics $UTHR is paying an $800 million cash upfront in a big bet to stay among the leaders in pulmonary arterial hypertension, grabbing rights to Arena Pharmaceuticals’ ralinepag in the deal. And the executive crew is willing to add hundreds of millions more in milestones if they can stay on track through to an approval and commercialization. [...]

By | 2018-11-19T14:17:18-04:00 November 15th, 2018|Daily Digest, News|Comments Off on United Therapeutics pays $800M-plus to grab Arena’s PhIII PAH drug

CSF-1 drops demonstrate efficacy, safety in clinical studies for treatment of presbyopia

Elad Kedar, CEO of Orasis Pharmaceuticals, provides a company update at OIS@AAO 2018 in Chicago.

By | 2018-11-28T11:56:40-04:00 November 14th, 2018|News, video|Comments Off on CSF-1 drops demonstrate efficacy, safety in clinical studies for treatment of presbyopia

Quantum Genomics’ brain-targeting blood pressure drug meets phase 2b endpoints

Quantum Genomics’ blood pressure drug firibastat, an inhibitor that targets aminopeptidase A in the brain, met its primary endpoint in a phase 2b study—which the company says paves the way for a wider phase 3 trial in more resistant hypertension.

By | 2018-11-13T11:19:21-04:00 November 12th, 2018|News|Comments Off on Quantum Genomics’ brain-targeting blood pressure drug meets phase 2b endpoints

Wnt is back in drugmakers’ sights, but is it druggable?

See author Cormac Sheridan's discussion of the biotech industry members developing therapeutics based on targeting the Wnt pathway in this issue of Nature Biotech. Included in the report is Samumed, a company developing a Wnt-targeted therapy for the treatment of Osteoarthritis and other prevalent diseases.

By | 2018-11-12T11:39:27-04:00 November 9th, 2018|News|Comments Off on Wnt is back in drugmakers’ sights, but is it druggable?

Clinical Challenges: Can OA Be Stopped?

A small-molecule intra-articular Wnt pathway inhibitor, SM04690, is being developed and the results of a phase IIb trial were presented at the ACR meeting by Yusuf Yazici, MD, of NYU Langone School of Medicine in New York City and Samumed, LLC, in San Diego.

By | 2018-11-07T16:27:08-04:00 November 7th, 2018|News|Comments Off on Clinical Challenges: Can OA Be Stopped?

Buoyed By Phase III Rosacea Success, Foamix Plans Commercial Transition

Market of dermatologists prescribing for rosacea and acne is very focused, so Foamix says it can manage commercialization of topical minocycline foam on its own.

By | 2018-11-08T15:46:52-04:00 November 7th, 2018|News|Comments Off on Buoyed By Phase III Rosacea Success, Foamix Plans Commercial Transition

Oxurion introduces new clinical portfolio at OIS

CHICAGO: At the Ophthalmology Innovation Summit at AAO, Patrik De Haes, MD, CEO of Oxurion, introduces the company’s new clinical portfolio with three separate molecules in clinical trials for the treatment of diabetic macular edema.

By | 2018-11-08T15:45:46-04:00 November 7th, 2018|News, video|Comments Off on Oxurion introduces new clinical portfolio at OIS

Going Public: A Guide for European Biotechs

“For Celyad, the sequence of listing first in Europe and then in the US allowed the company to first strengthen and solidify its company and clinical roots in Europe, and then broaden its investor base and support new programs by listing in the US,” Filippo Petti, CFO of Celyad, told me.

By | 2018-11-07T10:48:10-04:00 November 7th, 2018|News|Comments Off on Going Public: A Guide for European Biotechs

Developing Therapies to Fight Cancer and Autoimmune Diseases

We recently spoke to Alexis Peyroles, CEO at OSE Immunotherapeutics to hear more about the findings of their recent study, published in Nature Communications, describing, for the first time ever, the in vivo mechanism of action of interleukin 7 receptor alpha (IL-7Rα) monoclonal antibodies, suggesting therapeutic efficacy in controlling chronic inflammation.

By | 2018-11-07T10:44:15-04:00 November 7th, 2018|News|Comments Off on Developing Therapies to Fight Cancer and Autoimmune Diseases

Oxurion and Beta Therapeutics To Develop New Heparanase Inhibitors for Treatment of dry AMD

Oxurion announced that it entered into a strategic research collaboration with Beta Therapeutics (Canberra, Australia) to develop new heparanase inhibitors for the treatment of retinal disorders with large unmet medical needs such as dry age-related macular degeneration.

By | 2018-11-07T10:50:02-04:00 November 6th, 2018|News|Comments Off on Oxurion and Beta Therapeutics To Develop New Heparanase Inhibitors for Treatment of dry AMD

Morning Rounds – Pilot study finds medical cannabis tied to lower opioid use in chronic nerve pain patients

Taking medical cannabis led 62 percent of patients with chronic nerve pain to cut down or stop their opioid use, according to a first-of-its-kind pilot study that tracked 76 individuals over nine months.

By | 2018-10-31T13:57:06-04:00 October 31st, 2018|News|Comments Off on Morning Rounds – Pilot study finds medical cannabis tied to lower opioid use in chronic nerve pain patients

ProQR licenses Ionis’ RNA drug for inherited blindness

ProQR is licensing an RNA medicine from Ionis Pharmaceuticals for the treatment of retinitis pigmentosa, a form of rare, inherited blindness. The plan is to start a phase 1/2 trial of the drug in 2019.

By | 2018-10-29T11:45:53-04:00 October 29th, 2018|News|Comments Off on ProQR licenses Ionis’ RNA drug for inherited blindness

Patrik De Haes, MD: What’s Coming Down the Retina Pipeline

At the 2018 American Academy of Ophthalmology Annual Meeting in Chicago, IL, Patrik De Haes, MD, CEO of Oxurion (formerly ThromboGenics) spoke about several investigational molecules his company is investigating for various retina conditions.

By | 2018-10-29T09:45:25-04:00 October 28th, 2018|News|Comments Off on Patrik De Haes, MD: What’s Coming Down the Retina Pipeline

Expansion of Medical Marijuana Legalization

Columbia Care is the largest multi-state medical cannabis operator in the United States. With a total of 33 licenses in 13 states, the company is looking to make an impact in the global cannabis industry by partnering with Canaccord Genuity Growth. Nicholas Vita, CEO and co-founder of Columbia Care, joins Cheddar to discuss. [...]

By | 2018-10-23T09:57:12-04:00 October 22nd, 2018|News, video|Comments Off on Expansion of Medical Marijuana Legalization

Columbia Care CEO on Canada cannabis legalization

Nicholas Vita, Columbia Care CEO, discusses how Canada's legalization of recreational marijuana on Wednesday will affect the medicinal use market and how it may influence U.S.-based regulations.

By | 2018-10-17T16:04:54-04:00 October 16th, 2018|News, video|Comments Off on Columbia Care CEO on Canada cannabis legalization

Krystal Gains on Early Data for Topical Gene Therapy in Skin Blistering Disease

Krystal Biotech Inc. (NASDAQ:KRYS) added $4.32 (28%) to $20 on Monday when it reported interim data from the Phase I/II GEM trial showing that topical gene therapy KB103 met all primary efficacy and safety endpoints in two adults with recessive dystrophic epidermolysis bullosa.

By | 2018-10-15T17:06:22-04:00 October 15th, 2018|News|Comments Off on Krystal Gains on Early Data for Topical Gene Therapy in Skin Blistering Disease

This Biotech Has A Topical Gene Therapy — And Just Flew 30% On A Test

Krystal Biotech (KRYS) rocketed to a record high Monday after its gene therapy showed promise as a skin disease treatment. In midday trading on the stock market today, Krystal stock soared 30.9%, near 20.50. Earlier, Krystal popped as much as 37.6% in higher-than-average volume. Krystal stock began trading around 10 in September 2017.

By | 2018-10-15T15:56:41-04:00 October 15th, 2018|News|Comments Off on This Biotech Has A Topical Gene Therapy — And Just Flew 30% On A Test

FR104 offers control of graft-versus-host disease

In a game-changing preclinical study targeted toward controlling graft-versus-host disease (GvHD), OSE Immunotherapeutics SA has shown new efficacy results evaluating FR104 and whether a transplant takes. This study, announced Aug. 22, showed strong evidence in the value of targeting CD28 in GvHD for potential clinical applications in autoimmune diseases and transplantation.

By | 2018-10-11T14:07:03-04:00 October 11th, 2018|News|Comments Off on FR104 offers control of graft-versus-host disease

New Treatment for Obsessive-Compulsive Disorder with Dr. Nolan Williams

Dr. Nolan Williams, Clinical Assistant Professor of Psychiatry and Behavioral Sciences at Stanford University. We speak about new treatment options for use in treatment-resistant patients with OCD, including brain stimulation. A deep TMS device was recently FDA approved for the treatment of treatment-resistant OCD.

By | 2018-10-10T16:44:27-04:00 October 4th, 2018|listen, News|Comments Off on New Treatment for Obsessive-Compulsive Disorder with Dr. Nolan Williams

J&J hands Arrowhead a plum $3.7B deal for hep B-plus 3 — corralling a possible game-changing RNAi drug

Two years after Arrowhead Pharmaceuticals $ARWR conceded that a substantial segment of their RNAi pipeline was hopelessly compromised and had to be jettisoned, crippling their stock price, the biotech is staging a major comeback.

By | 2018-10-04T09:14:12-04:00 October 4th, 2018|News|Comments Off on J&J hands Arrowhead a plum $3.7B deal for hep B-plus 3 — corralling a possible game-changing RNAi drug

On A Roll: Arena Continues Streak Of Positive Data With Small Crohn’s Pain Study

Arena announced encouraging data from a small Phase IIa study for oloranib (APD371) in abdominal pain associated with Crohn's disease as the company continues a streak of good news after two of its more advanced clinical-stage programs posted positive results.

By | 2018-09-28T11:36:13-04:00 September 28th, 2018|News|Comments Off on On A Roll: Arena Continues Streak Of Positive Data With Small Crohn’s Pain Study

Twice as Splice

Abivax S.A. (Euronext:ABVX) has positioned its anti-HIV therapy ABX464 to take on inflammatory diseases after discovering the small molecule triggers RNA splicing that both halts HIV viral replication and boosts anti-inflammatory responses in HIV and ulcerative colitis. According to CEO Hartmut Ehrlich, ABX464 binds the human cap binding complex (CBC) and promotes its splicing [...]

By | 2018-09-28T10:22:23-04:00 September 27th, 2018|News|Comments Off on Twice as Splice