US ships out all remaining supplies of the only Covid treatment that works against Omicron

Right as the new Omi­cron vari­ant is poised to in­crease rapid­ly across the US, the fed­er­al gov­ern­ment has ef­fec­tive­ly run out of the on­ly mon­o­clon­al an­ti­body treat­ment that works against it, and at least one ma­jor hos­pi­tal sys­tem is now halt­ing all mAb in­fu­sions.

Late last month, the fed­er­al gov­ern­ment paused ship­ments of Glax­o­SmithK­line and Vir’s mAb treat­ment sotro­vimab in or­der to con­serve sup­plies of the on­ly treat­ment that might work against the Omi­cron vari­ant. Last week, how­ev­er, HHS told End­points News that the move to hold back sotro­vimab was un­re­lat­ed to Omi­cron, and due to a sur­plus of Eli Lil­ly mAbs, which aren’t ef­fec­tive against Omi­cron.

But late Fri­day, HHS con­firmed to End­points that the gov­ern­ment was with­hold­ing the sup­plies due to the Omi­cron vari­ant (and apol­o­gized for pro­vid­ing in­ac­cu­rate in­for­ma­tion a day ear­li­er).

HHS al­so si­mul­ta­ne­ous­ly an­nounced that it’s ship­ping its re­main­ing 55,000 dos­es of sotro­vimab, which will be­gin ar­riv­ing in the states on Tues­day un­til more sup­plies hope­ful­ly be­come avail­able the week of Jan. 3. The de­part­ment said in a state­ment:

Ear­ly in vit­ro da­ta sug­gests sotro­vimab works against the Omi­cron vari­ant. As such, we are ac­tive­ly prepar­ing ap­prox­i­mate­ly 55,000 dos­es of sotro­vimab for im­me­di­ate al­lo­ca­tion to state and ter­ri­to­r­i­al health de­part­ments. Ju­ris­dic­tions will be­gin re­ceiv­ing the prod­uct as ear­ly as Tues­day, De­cem­ber 21, 2021. Cur­rent sup­ply of sotro­vimab is lim­it­ed; how­ev­er, we ex­pect it to grow to ap­prox­i­mate­ly 300,000 ad­di­tion­al dos­es in Jan­u­ary. ‘The feds had no choice but to for­ward de­ploy the lim­it­ed stock­piles they have of the on­ly an­ti­body we know is like­ly to be high­ly po­tent against omi­cron,’ for­mer FDA com­mis­sion­er Scott Got­tlieb said.

But the about-face from HHS on why it was with­hold­ing sotro­vimab re­veals an agency scrap­ing to turn a mAb short­age in­to a pos­i­tive sto­ry about how it planned ahead.

In re­al­i­ty, very few hos­pi­tals na­tion­wide will have ad­e­quate sup­plies of sotro­vimab lat­er this week and next week, when cas­es will like­ly surge due to hol­i­day trav­el.

New York, Ohio, Penn­syl­va­nia, Michi­gan and Illi­nois were the on­ly states to re­ceive more than 3,000 dos­es of sotro­vimab each in the lat­est ship­ment.

And HHS is ad­vis­ing states to be cau­tious with its lim­it­ed sup­plies, adding, ‘Un­til lo­cal preva­lence of Omi­cron is greater than 20%, ju­ris­dic­tions are en­cour­aged to di­rect sotro­vimab to sites that can pro­vide IV treat­ment (with­in 48 hours of col­lec­tion of a pa­tient sam­ple) to high­est risk, el­i­gi­ble in­di­vid­u­als di­ag­nosed with a test that may iden­ti­fy a po­ten­tial case of the Omi­cron vari­ant.’

HHS al­so said Fri­day that the two oth­er avail­able mAbs, from Eli Lil­ly and Re­gen­eron, con­tin­ue to work against the Delta vari­ant, which re­mains the dom­i­nant strain in the US.

How­ev­er, the Mt. Sinai hos­pi­tal sys­tem in New York said late Sun­day that it’s sus­pend­ing in­fu­sions of the Lil­ly and Re­gen­eron mAbs due to Omi­cron.

‘Due to the in­creas­ing preva­lence of the Omi­cron vari­ant of SARS-CoV-2 and the lack of ef­fi­ca­cy of both bam­lanivimab/ete­se­vimab and casiriv­imab/imde­vimab, we have sus­pend­ed of­fer­ing these two treat­ments for treat­ment or for post-ex­po­sure pro­phy­lax­is,’ Mt. Sinai said in a state­ment.

Look­ing for­ward, states will have to pro­tect against Omi­cron with­out the mAb treat­ments, which will like­ly com­pound prob­lems for those who re­main un­vac­ci­nat­ed. Pend­ing FDA au­tho­riza­tion, two an­tivi­ral pills from Mer­ck and Pfiz­er, may al­so help against the new vari­ant, al­though it re­mains un­known how quick­ly those pills can be au­tho­rized and shipped out.

CALQUENCE is a registered trademark of the AstraZeneca group of companies.

At the 2021 American Society of Hematology (ASH) Annual Meeting & Exposition, blood cancer researchers from around the world gathered virtually to discuss the progress that has been made in the field of hematology. Over the past decade, that progress has been tremendous. We’ve seen not only breakthrough approaches to care, but also significant improvement upon existing novel treatments and exploring combinations within those medicines.1 These advances have transformed expectations of what a blood cancer diagnosis now means for patients. While we’ve come a long way, I believe the most exciting scientific discovery is yet to come, and that future advances will truly transform patient care.

Michel Vounatsos (Credit: World Economic Forum/Valeriano Di Domenico)

In a surprise move, Biogen announced Monday that it will cut in half the price of its controversial Alzheimer’s drug Aduhelm, slashing the cost from $56,000 to $28,000.

The sudden discount marks a sudden turnaround for the big biotech as it struggles to turn around a drug whose stuck-in-the-mud sales and political ramifications have sent the company into turmoil and triggered the ousting of its longtime chief scientist. Biogen’s leadership had resisted calls since June to reduce the price of the drug.

Unlock this story instantly and join 126,000+ biopharma pros reading Endpoints daily — and it’s free.

Stéphane Bancel, Moderna CEO (Andrew Harnik/AP Images)

Moderna has backed down on its patent fight with the NIH, calling a truce by dropping its patent application for now.

Following a heated feud regarding who invented its lifesaving Covid-19 vaccine that was increasingly spilling into public view, the biotech said it ‘has decided at this time not to pursue’ a patent issuance for the mRNA sequence of its jab. But Moderna also filed a continuation application so that some of the claims may still be issued later.

Unlock this story instantly and join 126,000+ biopharma pros reading Endpoints daily — and it’s free.

John Oyler, BeiGene CEO (Endpoints News, PharmCube)

Count Novartis in for the burgeoning TIGIT race.

After starting the year by plunking down $650 million upfront to license BeiGene’s PD-1 inhibitor — with positive Phase III data stacking up ever since — Novartis is returning to its biotech partner to pick up a Phase III TIGIT drug while entrusting it with marketing five of its approved cancer treatments in China.

The structure of the deal is reminiscent of the 2017 Celgene pact that put BeiGene on the map, which also saw the partners swap an experimental compound for commercial operations.

Unlock this story instantly and join 126,000+ biopharma pros reading Endpoints daily — and it’s free.

Tim Van Hauwermeiren, argenx CEO

If you look on argenx’s website today, you’ll see a burst of confetti. That’s because — in addition to getting a new type of therapy past the FDA for patients with a chronic neuromuscular disease called myasthenia gravis — the company is celebrating its first drug approval.

Regulators on Friday gave the thumbs up to argenx’s efgartigimod, now marketed as Vyvgart, for patients with generalized myasthenia gravis (gMG) who test positive for the anti-acetylcholine receptor (AChR) antibody. CEO Tim Van Hauwermeiren said in a statement that the approval triggers the ‘start of a new era for argenx.’

Welcome back to Endpoints Weekly, your review of the week’s top biopharma headlines. Want this in your inbox every Saturday morning? Current Endpoints readers can visit their reader profile to add Endpoints Weekly. New to Endpoints? Sign up here.

As JP Morgan moves #JPM22 fully virtual, so will Endpoints News. We’re taking our multi-day hybrid event schedule online, with no live cocktail hour or networking events but plenty of timely news, insightful panels and fireside chats previewing the new year. We’ll be sad to not see our friends and colleagues on site, but we encourage everyone to still register for the event and join the conversation.

Unlock this story instantly and join 126,000+ biopharma pros reading Endpoints daily — and it’s free.

A nurse administers a COVID-19 booster shot to Joe Rigdon at a vaccination site in Eastmonte Park, Altamonte Springs. (Photo by Paul Hennessy/SOPA Images/LightRocket via Getty Images)

When Laura Burns went to get her first Covid-19 shot last January, no one had warned her that the vaccines might not work for her.

Burns, the recipient of a double-lung transplant in 2016, knew to be careful about the medicines she took. She consulted with her transplant team when the Pfizer and Moderna shots were authorized and only signed up after being told the vaccines would likely be safe for her, which they were.

Unlock this story instantly and join 126,000+ biopharma pros reading Endpoints daily — and it’s free.

Richard Pazdur (via AACR)

There’s no denying that Merck’s Keytruda set a high bar for checkpoint inhibitors in development everywhere. But when it comes to the often redundant development of PD(L)-1 antibodies worldwide, FDA’s top cancer doctors Rick Pazdur and Julia Beaver are calling for more industry coordination.

‘Efforts to corral this enthusiasm should focus on increased international partnerships between sponsors of approved checkpoint inhibitors and those developing novel agents to be used with anti–PD-1 and anti–PD-L1 antibodies rather than developing ‘me too’ drugs,’ Beaver and Pazdur wrote Wednesday in the New England Journal of Medicine.

Unlock this story instantly and join 126,000+ biopharma pros reading Endpoints daily — and it’s free.

The FDA on Wednesday not only approved the first generic versions of the decades-old diabetes insipidus treatment vasopressin, but also simultaneously offered a particularly damning rebuke of a citizen petition attempting to block the generic, while promising to pass along the matter to the Federal Trade Commission.

The response could prove troublesome for the sponsor of the brand name version of the drug, Endo’s Par Sterile Products, which brought in more than $780 million in 2020 for its brand name version of the drug Vasostrict.
https://endpts.com/us-ships-out-all-remaining-supplies-of-the-only-covid-treatment-that-works-against-omicron/