Pfiz­er Foun­da­tion of­fers $2M in grants to NGOs tack­ling an­timi­cro­bial re­sis­tance; Bio­gen, In­vi­tae join forces to de­vel­op faster SMA di­ag­nos­tic

→ Most of Big Phar­ma has left the build­ing when it comes to an­timi­cro­bial drug de­vel­op­ment, and small com­pa­nies with new­ly ap­proved an­tibi­otics are strug­gling to stay afloat. Mean­while, the foun­da­tion arm of Pfiz­er $PFE is of­fer­ing its sup­port, in the form of grants for NGO and so­cial en­ter­pris­es that are work­ing on ad­dress­ing this ma­jor health chal­lenge: an­timi­cro­bial re­sis­tance. Re­cip­i­ents of the one-year Glob­al Health In­no­va­tion Grants in­clude part­ners in 12 low- and mid­dle-in­come coun­tries who will each re­ceive $100,000. 

→ While Bio­gen‘s $BI­IB spinal mus­cu­lar at­ro­phy treat­ment, Spin­raza, ri­vals No­var­tis$NVS gene-ther­a­py Zole­gens­ma, the US drug­mak­er has tied up with ge­net­ics com­pa­ny In­vi­tae $NV­TA to ush­er in a new ge­net­ic test for SMA, which will be of­fered at no charge to in­di­vid­u­als in the Unit­ed States as part of the SMA Iden­ti­fied pro­gram. The test re­duces the time need­ed for ge­net­ic test­ing to help con­firm a de­fin­i­tive SMA di­ag­no­sis to 4 days from 21, en­abling ear­li­er treat­ment for the of­ten life-threat­en­ing dis­ease, the com­pa­nies said on Tues­day.  

→ In its lat­est H1 re­port, Hong Kong-list­ed WuXi Vac­cines, a joint ven­ture of WuXi Bi­o­log­ics and Shang­hai Hile Bio-Phar­ma­ceu­ti­cal, in­di­cat­ed it had en­tered in­to a longterm man­u­fac­tur­ing part­ner­ship with an un­named glob­al vac­cine com­pa­ny. The com­pa­ny es­ti­mates the val­ue of the 20-year con­tract to be over $3 bil­lion. WuXi is aim­ing to fi­nal­ize the con­tract this year and ex­pects it will make a “sub­stan­tial” rev­enue con­tri­bu­tion in 2022.

→ Late last year, af­ter their drug uben­imex proved to be an­oth­er flop, Eiger Phar­ma­ceu­ti­cals $EIGR CEO David Cory said that the com­pa­ny would be reshuf­fling and fo­cus­ing on, among oth­er things, its late-stage study in he­pati­tis delta virus (HDV), the most se­vere form of hu­man vi­ral he­pati­tis for which there is no ap­proved ther­a­py. On Tues­day, Eiger an­nounced that the FDA had grant­ed break­through ther­a­py des­ig­na­tion for the com­pa­ny’s ex­per­i­men­tal drug, pegin­ter­fer­on lamb­da, to treat HDV, sup­port­ed by da­ta from a mid-stage study in 33 HDV-in­fect­ed pa­tients.  

iBio has inked a mas­ter ser­vices agree­ment (MSA) agree­ment with Unit­ed Ther­a­peu­tics sub­sidiary, Lung Biotech­nol­o­gy. Un­der the agree­ment, the com­pa­ny will pro­duce re­com­bi­nant hu­man col­la­gen (“rhCol­la­gen”)-based bioink for 3D bio­print­ed or­gan trans­plants. IBio will col­lab­o­rate with its part­ner to scale-up pro­duc­tion of rhCol­la­gen in to­bac­co plants us­ing iBio’s Fast­Pharm­ing Sys­tem — which com­bines plant pro­tein ex­pres­sion, au­to­mat­ed hy­dro­pon­ics, and gly­can en­gi­neer­ing tech­nolo­gies. The com­pa­ny is al­so look­ing to de­vel­op their own pipeline, with a lead as­set, CFB-03, for the treat­ment of fi­brot­ic dis­eases.

Scott Gottlieb, AP Images

Scott Got­tlieb is once again join­ing a team that en­joyed good times at the FDA un­der his high-en­er­gy stint at the helm

Right after jumping on Michael Milken’s FasterCures board on Monday, the newly departed FDA commissioner is back today with news about another life sciences board post that gives him a ringside chair to cheer on a lead player in the real-world evidence movement — one with very close ties to the FDA.

Aetion is reporting this morning that Gottlieb is joining their board, a group that includes Mohamad Makhzoumi, a general partner at New Enterprise Associates, where Gottlieb returned after stepping out of his role at the FDA 2 years after he started.

Gottlieb — one of the best connected execs in biopharma — knows this company well. As head of FDA he championed the use of real-world evidence to help guide drug developers and the agency in gaining greater efficiencies, which helped set up Aetion as a high-profile player in the game.

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Deborah Dunsire. Lundbeck

UP­DAT­ED: Deb­o­rah Dun­sire is pay­ing $2B for a chance to leap di­rect­ly in­to a block­buster show­down with a few of the world's biggest phar­ma gi­ants

A year after taking the reins as CEO of Lundbeck, Deborah Dunsire is making a bold bid to beef up the Danish biotech’s portfolio of drugs in what will likely be a direct leap into an intense rivalry with a group of giants now carving up a growing market for new migraine drugs.

Bright and early European time Monday morning the company announced that it will pay up to about $2 billion to buy Alder, a little biotech that is far along the path in developing a quarterly IV formulation of a CGRP drug aimed at cutting back the number of crippling migraines patients experience each month. In a followup call, Dunsire also noted that the company will likely need 200 to 250 reps for this marketing task on both sides of the Atlantic. And analysts were quick to note that the dealmaking at Lundbeck isn’t done, with another $2 billion to $3 billion available for more deals to beef up the pipeline.

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San Diego cou­ple charged with steal­ing trade se­crets, open­ing Chi­nese biotech as DOJ crack­down con­tin­ues

A San Diego couple has been charged with stealing trade secrets from a US hospital and opening a business based off those secrets in China as the controversial industry-wide crackdown on alleged corporate espionage continues. On the same day, the Department of Justice announced they had arrested Beijing representative Zhongsan Liu for allegedly trying to obtain research visas for government recruiters.

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UP­DAT­ED: Bio­gen pulls the plug on prized IPF drug from $562M+ Stromedix buy­out

One of Biogen’s attempts to branch out has flopped as the biotech scraps a mid-stage program for idiopathic pulmonary fibrosis.

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Tower Bridge in London [Shutterstock]

#UK­BIO19: Join GSK’s Hal Bar­ron and a group of top biotech ex­ecs for our 2nd an­nu­al biotech sum­mit in Lon­don

Over the past 10 years I’ve made a point of getting to know the Golden Triangle and the special role the UK biopharma industry plays there in drug development. The concentration of world class research institutes, some of the most accomplished scientists I’ve ever seen at work and a rising tide of global investment cash leaves an impression that there’s much, much more to come as biotech hubs are birthed and nurtured.

It’s fi­nal­ly over: Bio­gen, Ei­sai scrap big Alzheimer’s PhI­I­Is af­ter a pre­dictable BACE cat­a­stro­phe rais­es safe­ty fears

Months after analysts and investors called on Biogen and Eisai to scrap their BACE drug for Alzheimer’s and move on in the wake of a string of late-stage failures and rising safety fears, the partners have called it quits. And they said they were dropping the drug — elenbecestat — after the independent monitoring board raised concerns about…safety.

We don’t know exactly what researchers found in this latest catastrophe, but the companies noted in their release that investigators had determined that the drug was flunking the risk/benefit analysis.

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Warts for the win: Aclar­is' lead drug clears piv­otal study

Aclaris Therapeutics has found a way to get rid of the warts and all.

The company — which earlier this month decided to focus on its arsenal of kinase inhibitors — on Monday unveiled positive data from a pivotal study testing its lead experimental drug for use in common warts.

The drug, A-101, was tested in a 502-patient study called THWART-2 — patients enrolled had one to six warts before qualifying for the trial. Patients either self-administered A-101 topical solution or a vehicle twice a week over a two-month period. A higher proportion of patients on the drug (a potent hydrogen peroxide topical solution) saw their warts disappear at day 60, versus the vehicle (p<0.0001) — meeting the main goal of the study.  Each secondary endpoint also emerged in favor of A-101, the company said.

Charles Nichols, LSU School of Medicine

Could psy­che­delics tack­le the obe­si­ty cri­sis? A long­time re­searcher in the field says his lat­est mouse study sug­gests po­ten­tial

Psychedelics have experienced a renaissance in recent years amid a torrent of preclinical and clinical research suggesting it might provide a path to treat mood disorders conventional remedies have only scraped at. Now a preclinical trial from a young biotech suggests at least one psychedelic compound has effects beyond the mind, and — if you believe the still very, very early hype — could provide the first single remedy for some of the main complications of obesity.

Ac­celeron drops a de­vel­op­ment pro­gram as #2 drug fails to spark func­tion­al ben­e­fits in pa­tients with a rare neu­ro­mus­cu­lar ail­ment

Acceleron is scrapping a muscular dystrophy development program underway for its number 2 drug in the pipeline after pouring over some failed mid-stage secondary data.

Gone is the ACE-083 project in patients with facioscapulohumeral muscular dystrophy. Their drug hit the primary endpoint on building muscle but flopped on key secondaries for functional improvements in patients, which execs felt was vital to the drug’s success.