Gilead ups its bet on HIV, hep B, ink­ing $400M part­ner­ship with im­munother­a­py com­pa­ny Hookipa

In search of new as­sets to bol­ster its lead­ing HIV fran­chise, Gilead is en­list­ing the help of im­munother­a­py spe­cial­ists at Hookipa Biotech to bring in some fresh R&D.

Topped with $10 mil­lion up­front and worth up to $400 mil­lion, the deal gives Gilead ex­clu­sive ac­cess to Hookipa’s are­navirus vec­tor-based im­mu­niza­tion tech­nolo­gies, Vaxwave and Ther­aT. As well as HIV, the Fos­ter City, CA-based big biotech will al­so take a crack at he­pati­tis B us­ing these vi­ral plat­forms.

Jo­ern Aldag

Vi­en­na-based Hookipa is not known for their HBV and HIV ef­forts, hav­ing cho­sen to fo­cus on cy­tomegalovirus in­fec­tion for their sole clin­i­cal pro­gram and tout the po­ten­tial of its Ther­aT plat­form to elic­it T cells re­sponse in can­cer. Back in De­cem­ber, it raised $60 mil­lion in Se­ries C cap­i­tal to push the CMV drug can­di­date in­to Phase II. Gilead was a strate­gic in­vestor in that fi­nanc­ing.

“This part­ner­ship is strong recog­ni­tion of our unique im­mu­niza­tion tech­nol­o­gy, and helps us con­cen­trate our own en­er­gy and re­sources on im­muno-on­col­o­gy,” said Hookipa CEO Jo­ern Aldag in a state­ment. “The col­lab­o­ra­tive HIV and HBV pro­grams nice­ly com­ple­ment our sig­nif­i­cant ef­forts in the in­fec­tious dis­ease area with an ex­cit­ing pro­pri­etary pro­phy­lac­tic CMV vac­cine.”

Bill Lee

A look at its pipeline sug­gests that Hookipa’s at dis­cov­ery stage with both the HIV and HBV as­sets. Gilead is pick­ing up the tab for all re­search and de­vel­op­ment ac­tiv­i­ties, which it says will be a joint en­deav­or be­tween the part­ners. Hookipa is in charge of man­u­fac­tur­ing the vi­ral vec­tors used in clin­i­cal de­vel­op­ment.

The ear­ly-stage col­lab­o­ra­tion builds on a long his­to­ry of HIV — and vi­ral he­pati­tis — drug de­vel­op­ment at Gilead, whose triplet oral ther­a­py Bik­tarvy just got ap­proved a few months ago with a $6 bil­lion peak sales es­ti­mate.

“We are con­vinced that Hookipa’s unique ther­a­peu­tic vac­cine tech­nol­o­gy, which has demon­strat­ed ex­cel­lent safe­ty and im­muno­genic­i­ty in Phase I clin­i­cal stud­ies, has strong po­ten­tial to have syn­er­gis­tic ef­fect with oth­er Gilead cure ef­forts in both of these dis­eases ar­eas,” said Bill Lee, Gilead’s EVP of re­search.

Biotech Half­time Re­port: Af­ter a bumpy year, is biotech ready to re­bound?

The biotech sector has come down firmly from the highs of February as negative sentiment takes hold. The sector had a major boost of optimism from the success of the COVID-19 vaccines, making investors keenly aware of the potential of biopharma R&D engines. But from early this year, clinical trial, regulatory and access setbacks have reminded investors of the sector’s inherent risks.

RBC Capital Markets recently surveyed investors to take the temperature of the market, a mix of specialists/generalists and long-only/ long-short investment strategies. Heading into the second half of the year, investors mostly see the sector as undervalued (49%), a large change from the first half of the year when only 20% rated it as undervalued. Around 41% of investors now believe that biotech will underperform the S&P500 in the second half of 2021. Despite that view, 54% plan to maintain their position in the market and 41% still plan to increase their holdings.

Covid-19 vac­cine boost­ers earn big thumbs up, but Mod­er­na draws ire over world sup­ply; What's next for Mer­ck’s Covid pill?; The C-suite view on biotech; and more

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.

You may remember that at the beginning of this year, Endpoints News set a goal to go broader and deeper. We are still working towards that, and are excited to share that Beth Snyder Bulik will be joining us on Monday to cover all things pharma marketing. You can sign up for her weekly Endpoints MarketingRx newsletter in your reader profile.

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No­var­tis de­vel­op­ment chief John Tsai: 'We go deep in the new plat­form­s'

During our recent European Biopharma Summit, I talked with Novartis development chief John Tsai about his experiences over the 3-plus years he’s been at the pharma giant. You can read the transcript below or listen to the exchange in the link above.

John Carroll: I followed your career for quite some time. You’ve had more than 20 years in big pharma R&D and you’ve obviously seen quite a lot. I really was curious about what it was like for you three and a half years ago when you took over as R&D chief at Novartis. Obviously a big move, a lot of changes. You went to work for the former R&D chief of Novartis, Vas Narasimhan, who had his own track record there. So what was the biggest adjustment when you went into this position?

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Susan Galbraith, Executive VP, Oncology R&D, AstraZeneca

As­traZeneca on­col­o­gy R&D chief Su­san Gal­braith: 'Y­ou're go­ing to need or­thog­o­nal com­bi­na­tion­s'

 

Earlier in the week we broadcast our 4th annual European Biopharma Summit with a great lineup of top execs. One of the one-on-one conversations I set up was with Susan Galbraith, the oncology research chief at AstraZeneca. In a wide-ranging discussion, Galbraith reviewed the cancer drug pipeline and key trends influencing development work at the pharma giant. You can watch the video, above, or stick with the script below. — JC

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Roche's Tecen­triq cross­es the fin­ish line first in ad­ju­vant lung can­cer, po­ten­tial­ly kick­ing off gold rush

While falling behind the biggest PD-(L)1 drugs in terms of sales, Roche has looked to carve out a space for its Tecentriq with a growing expertise in lung cancer. The drug will now take an early lead in the sought-after adjuvant setting — but competitors are on the way.

The FDA on Friday approved Tecentriq as an adjuvant therapy for patients with Stage II-IIIA non small cell lung cancer with PD-(L)1 scores greater than or equal to 1, making it the first drug of its kind approved in an early setting that covers around 40% of all NSCLC patients.

Amit Etkin, Alto Neuroscience CEO (Alto via Vimeo)

A star Stan­ford pro­fes­sor leaves his lab for a start­up out to re­make psy­chi­a­try

About five years ago, Amit Etkin had a breakthrough.

The Stanford neurologist, a soft-spoken demi-prodigy who became a professor while still a resident, had been obsessed for a decade with how to better define psychiatric disorders. Drugs for depression or bipolar disorder didn’t work for many patients with the conditions, and he suspected the reason was how traditional diagnoses didn’t actually get at the heart of what was going on in a patient’s brain.

Susan Galbraith speaking at Endpoints News' virtual EUBIO21 summit

Imfinzi/treme­li­mum­ab com­bo scores As­traZeneca an­oth­er OS win — this time in liv­er can­cer

Is the tide turning on AstraZeneca’s battered PD-L1/CTLA4 combo?

A single priming dose of the experimental tremelimumab, followed by Imfinzi every four weeks, beat Nexavar (sorafenib) in helping a group of liver cancer patients live longer in a Phase III study, the company reported, meeting the primary endpoint.

Specifically, the two drugs extended overall survival for patients with unresectable hepatocellular carcinoma who had not received prior systemic therapy and were not eligible for localized treatment.

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FDA+ roundup: Marks on Wood­cock­'s tenure as act­ing com­mis­sion­er; FDA lead­ers of­fer per­spec­tive on bar­ri­ers to di­ver­si­ty in re­search

CBER director Peter Marks praised Janet Woodcock’s work as acting FDA commissioner, and while noting that Biden needs to nominate someone to fill the role permanently by Nov. 16, he said he has “no idea” when that actually might occur.

“Dr. Woodcock has been at the agency for over three decades and she, during that time, has proven herself to be a remarkably capable manager,” Marks said at the Alliance for Regenerative Medicine’s meeting Tuesday. “And she’s been managing as if she’s commissioner, unlike some previous acting [commissioners] who are afraid to actually do things. She doesn’t appear to be afraid to do things. I have not felt any different now from when we had a commissioner in place,” he added.

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FDA ad­comm votes unan­i­mous­ly in sup­port of a J&J Covid-19 boost­er two months af­ter one-dose shot

The FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) on Friday voted 19-0 in favor of authorizing a second shot of J&J’s Covid-19 vaccine to follow at least two months after the initial dose.

Regulators don’t have to follow VRBPAC’s recommendation, but they almost always do. Considering that the CDC’s advisory committee has already been set to review the expanded EUA, VRBPAC’s recommendation is likely to be adopted.