Neil Woodford. Woodford Investment Management via YouTube

Neil Wood­ford re­fresh­es port­fo­lio with fire sale while in­vestors pon­der fu­ture of sus­pend­ed fund

Ahead of an ex­pect­ed up­date on the sus­pen­sion of his flag­ship fund, Neil Wood­ford has re­port­ed­ly raised £459 mil­lion from share sales across his port­fo­lio of funds, City­wire re­ports.

The in­vest­ment man­age­ment firm is hold­ing some of it in cash while putting the rest to use in oth­er stocks, a spokesper­son told Bloomberg — which counts at least £300 mil­lion ($379 mil­lion) in sales from the frozen Eq­ui­ty In­come Fund. Sell­ing off illiq­uid or un­list­ed as­sets is key to Wood­ford’s turn­around mis­sion for the fund, which was suf­fer­ing from an ex­o­dus of in­vestors that shrunk the fund from £10.2 bil­lion to £3.7 bil­lion in two years and squeezed its abil­i­ty to meet any fur­ther re­demp­tions.

“We haven’t dis­put­ed the City­wire or Bloomberg sto­ries, but we do not pro­vide con­fir­ma­tion of every sale or stock bought by Wood­ford,” a spokesper­son told me in re­sponse to a query. “The de­ci­sion on sus­pen­sion is made by Link, the ACD for the fund, and I be­lieve they are plan­ning to make an an­nounce­ment lat­er to­day.”

Link Fund So­lu­tions is tech­ni­cal­ly the “au­tho­rized cor­po­rate di­rec­tor” that del­e­gat­ed Wood­ford’s firm to man­age its funds.

Af­ter abrupt­ly no­ti­fy­ing in­vestors that they would not be al­lowed to re­deem, sell, trans­fer or can­cel their shares in the Wood­ford Eq­ui­ty In­come Fund for at least 28 days, Wood­ford ex­plained that he need­ed the time and re­sources to re­bal­ance the port­fo­lio. To­day marks the end of that four-week time­frame.

Through pub­lic fil­ings and da­ta, Bloomberg found that since dis­clos­ing the dras­tic mea­sure in June, he has sold shares in BCA Mar­ket­place, NewRiv­er RE­IT and Oak­ley Cap­i­tal In­vest­ments, among oth­er po­si­tions.

On top of that, he’s al­so of­floaded stakes in Mereo Bio­phar­ma, e-Ther­a­peu­tics and Sen­syne Health, ac­cord­ing to City­wire. Some sales had ap­par­ent­ly come from the Wood­ford In­come Fo­cus Fund, which is still open and has lost in­vestors de­spite Wood­ford’s best ef­forts. The Pa­tient Cap­i­tal Trust is al­so ex­plor­ing sales af­ter trad­ing down al­most 30% on the Lon­don Stock Ex­change, in part to help cut bor­row­ing.

Days ago, UK fi­nan­cial reg­u­la­tors say they are now tak­ing a hard look in­to the sus­pen­sion of the Eq­ui­ty Fund. How Wood­ford man­aged the liq­uid­i­ty of the fund will like­ly be the cen­ter of the Fi­nan­cial Con­duct Au­thor­i­ty’s scruti­ny.

As in­vestors anx­ious­ly await an up­date, the Times is re­port­ing that Link plans to con­tin­ue the sus­pen­sion in­def­i­nite­ly be­cause they deem the Eq­ui­ty Fund un­pre­pared for the flood of ex­pect­ed re­demp­tion re­quests.

We will be watch­ing for the of­fi­cial re­lease when it drops.

Com­mu­ni­cat­ing the val­ue of pre­ci­sion med­i­cine

By Natasha Cowan, Content Marketing Manager at Blue Latitude Health.
Many stakeholders are confused by novel precision medicines, including patients and healthcare professionals. So, how can industry help them to navigate this complexity?

Precision medicine represents a new paradigm in healthcare. It embodies the shift from treating many patients with the same therapy, to having the tools to identify the best treatment for every patient.

(Image: Associated Press)

Amarin emerges from an ex­pert pan­el re­view with a clear en­dorse­ment for Vas­cepa and high odds of suc­cess when the FDA weighs in for­mal­ly

Several FDA experts who gathered Thursday to consider the landmark approval of Vascepa to reduce cardio events in an at-risk population voiced their unease about various aspects of the efficacy and safety data, or ultimately the population it should be used to treat. But the overwhelming belief that the data pointed to the drug’s benefit and clearly outweighed risks carried the day for Amarin.

The panel voted unanimously (16 to 0) to support the company’s positive data presentation — backing an OK for expanding the label to include reducing cardio risk. The vote points Amarin $AMRN down a short path to a formal decision by the FDA, with the odds heavily in its favor. Chances are the rest of the questions about the future of this drug will be hashed out in the label’s small print.

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What does $62B buy you these days? A lot, says Take­da ex­ecs as the phar­ma play­er promis­es a block­buster R&D fu­ture

First comes the $62 billion buyout. Then comes the asset auction and reorganization to pay down debt. Now comes the detailed pledge of a bigger, brighter future in drug development.

That’s where Takeda finds itself on R&D day today, about 11 months after closing on their Shire acquisition. R&D chief Andy Plump is joining CEO Christophe Weber and other top members of the team to outline a new set of priorities in the greatly expanded pipeline at Takeda, which has jumped into the top ranks of the world’s pharma giants in the wake of the Shire deal.

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BeiGene CEO John Oyler at an Endpoints event in Shanghai, October 2018 (Credit: Endpoints News/PharmCube)

UP­DAT­ED: Chi­na's BeiGene scores first-ever FDA ap­proval — but can they carve up J&J's block­buster fran­chise?

Weeks after Amgen took a $2.7 billion stake in BeiGene, the Beijing-based biotech has secured its first-ever FDA approval for zanubrutinib, a BTK inhibitor, months ahead of schedule.

BeiGene’s drug, branded as Brukinsa, has secured accelerated approval for adult patients with mantle cell lymphoma (MCL) — a typically aggressive, rare, form of blood cancer — who have received at least one prior therapy.

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Spe­cial re­port: Twen­ty ex­tra­or­di­nary women in bio­phar­ma R&D who worked their way to the top

What differentiates a woman leader in biopharma R&D from a man?

Not much, except there are fewer of them in senior posts. Data suggest women are not more risk-averse, family-oriented or less confident than their male counterparts — indeed the differences between the two sexes are negligible. But a glance at the top R&D positions in Big Pharma leaves little doubt that upward migration in the executive ranks of biopharma R&D is tough.

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GSK's asth­ma bi­o­log­ic Nu­cala scores in rare blood dis­or­der study

GlaxoSmithKline’s asthma drug Nucala, which received a resounding FDA rejection for use in chronic obstructive pulmonary disease (COPD) last year, has shown promise in a rare blood disorder.

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Mer­ck buys a fledg­ling neu­rode­gen­er­a­tive biotech spawned by an old GSK dis­cov­ery al­liance. What’s up with that?

Avalon Ventures chief Jay Lichter has a well-known yen for drug development programs picked up in academia. And what he found in Haoxing Xu’s lab at the University of Michigan pricked his interest enough to launch one of his umbrella biotechs in San Diego.

Xu’s work laid the foundation for Avalon to launch Calporta, which has been working on finding small molecule agonists of TRPML1 (transient receptor potential cation channel, mucolipin subfamily, member 1) for lysosomal storage disorders. And that pathway, they believe, points to new approaches on major market neurodegenerative diseases like Parkinson’s, ALS and Alzheimer’s.

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Carson Block. Muddy Waters via YouTube

Shorts ga­lore: Mud­dy Wa­ters sees slide for Pep­tiDream, tweets con­cerns about Fi­bro­Gen's new da­ta

The short seller Muddy Waters is taking aim at Japan’s most profitable biotech, projecting a slide for a company that has skyrocketed over the last four years. Meanwhile, the firm tweeted out an analysis accusing FibroGen of manipulating data to obscure safety concerns in their latest reveal, although some investors seem satisfied by the biotech’s explanation.

Muddy Waters shorted PeptiDream, a Japanese biotech-for-hire that leveraged its peptide library into partnerships with some of the world’s largest pharmaceutical companies, a 50% profit margin and $6 billion valuation. The firm noted that despite its esteem, PeptiDream has failed to bring a drug to market 13 years after its 2006 launch (although this is not especially rare for biotech).

Pin­cer move­ment: Cal­i­for­nia biotech gets $35M to suf­fo­cate can­cer in co­or­di­nat­ed at­tack

Having served in Afghanistan, the navy veteran leading California-based EpicentRx wants to leave no patient behind with his arsenal of anti-cancer drugs. On Thursday, the company was given a $35 million boost to further its mission.

The injection of funds will be used to shepherd its late-stage CD47 drug, RRx-001, to the FDA for marketing, and its oncolytic virus program into the clinic.

RRx-001, engineered as an agent that makes tumor cells more sensitive to therapy, is in a Phase III trial in combination with chemotherapy for use in third-line and beyond small cell lung cancer (SCLC). The drug has been granted orphan drug designation from FDA for SCLC, neuroendocrine cancer and glioblastoma.