Pe­ter Dia­man­dis' right hand man Sergey Young wants to re­verse ag­ing via his $100M Longevi­ty Vi­sion Fund

In­spired by British bil­lion­aire Jim Mel­lon, chair­man of an­ti-ag­ing up­start biotech ven­ture Ju­ve­nes­cence, Sergey Young un­veiled a $100 mil­lion fund on Mon­day to cat­alyze the de­vel­op­ment of a com­pre­hen­sive so­lu­tion to coun­ter­act the dam­ag­ing con­se­quences of ag­ing.

“I’ve nev­er looked like my age…and with my name, I think it was pre­de­ter­mined that I was go­ing to work in the space (of ag­ing),” Young told End­points News. The 47-year-old con­sid­ers him­self a prod­uct of Pe­ter Dia­man­dis — the man be­hind the non-prof­it XPRIZE and ven­ture cap­i­tal fund BOLD Cap­i­tal Part­ners — and is in charge of all things longevi­ty at both or­ga­ni­za­tions.

Jim Mel­lon

Like Mel­lon, who penned Ju­ve­nes­cence: In­vest­ing in the Age of Longevi­ty pri­or to the launch of the com­pa­ny Ju­ve­nes­cence, Young is in the em­bry­on­ic stage of writ­ing his own book de­signed to de­code the sci­ence of ag­ing for the mass­es. Mean­while, his $100 mil­lion Longevi­ty Vi­sion Fund will back or­ga­ni­za­tions who are work­ing on tech­nol­o­gy to re­verse the ag­ing process and pro­long healthy hu­man life.

“Adding 20 to 30 healthy years on a per­son’s life is like­ly to be the largest mar­ket op­por­tu­ni­ty on earth. The con­ver­gence of Genome Se­quenc­ing, AI & Cel­lu­lar Med­i­cine will en­able break­throughs that will make 100 years old the new 60. I’m proud through our BOLD Cap­i­tal part­ner­ship to sup­port Sergey Young and the Longevi­ty Vi­sion Fund,” Pe­ter Dia­man­dis said in a state­ment.

Young did not dis­close the deals his fund is cur­rent­ly ex­plor­ing but laid out the ar­eas he is in­ter­est­ed in pur­su­ing.

Pe­ter Dia­man­dis

“We are cur­rent­ly work­ing on 6 deals…and are look­ing at all the usu­al sus­pects in terms of themes” he said. These ar­eas in­clude ear­ly de­tec­tion of se­ri­ous dis­eases us­ing ul­tra­sound tech­nol­o­gy; ear­ly di­ag­nos­tics for heart, can­cer and neu­rode­gen­er­a­tive dis­eases; stem-cell and mi­cro­bio­me-based ther­a­peu­tics; and big da­ta as well as AI-based ap­pli­ca­tions.

Un­sur­pris­ing­ly, Young is in di­a­logue with Alex Zha­voronkov’s AI shop at In­sil­i­co Med­i­cine. Zha­voronkov has deep con­nec­tions in the R&D space — last year he raised funds at the be­hest of Shang­hai high-fly­er WuXi AppTec, Sin­ga­pore’s Temasek, Pe­ter Dia­man­dis and Ju­ve­nes­cence.

“We do plan to par­tic­i­pate in the next round of fund­ing to be­come a share­hold­er of In­sil­i­co,” Young said. It is a mu­tu­al ap­pre­ci­a­tion so­ci­ety here at the Longevi­ty Lead­ers Con­gress in Lon­don, where Zha­voronkov is heard in­tro­duc­ing Young as a vi­sion­ary fund man­ag­er to a con­fer­ence at­tendee. Young, Zha­voronkov, Mel­lon and a host of oth­ers high-pro­file C-suite reg­u­lars in­volved in ag­ing R&D have flocked to a ho­tel near the renowned St Paul’s Cathe­dral to dis­cuss re­cent de­vel­op­ments in an­ti-ag­ing. In the first keynote pan­el of the day, vice pres­i­dent of Ju­ve­nes­cence-backed AgeX Aubrey de Grey am­bi­tious­ly claims that that longevi­ty space will even­tu­al­ly “dwarf the dot­com boom.”

Alex Zha­voronkov

But more fund­ing is nec­es­sary, Zha­voronkov told End­points News at the con­fer­ence. Oth­er than Google’s an­ti-ag­ing biotech Cal­i­co that has seen a large in­flux of funds, the field of an­ti-ag­ing is ripe for in­vest­ment, he said.

For long-time in­vestor and ven­ture cap­i­tal­ist Young, who has in­sight in­to the ag­ing R&D ef­fort with­in the US and to a less­er ex­tent in the UK, Chi­na and In­dia’s siz­able pop­u­la­tions pose com­pelling prospects for deals for his fund.

“In the next decade, ad­vance­ments will al­low us to be a lot more pre­dic­tive and pre­ven­ta­tive in the most dam­ag­ing dis­eases,” he said. “I’m think­ing AI-en­abled med­i­cine will em­pow­er doc­tors…tech­no­log­i­cal ad­vances to im­prove sleep­ing and med­i­ta­tion will emerge — and these are an es­sen­tial part of a healthy, long life, along with a plant-based di­et.”


Im­age: Sergey Young. LONGEVI­TY VI­SION FUND

M&A: a crit­i­cal dri­ver for sus­tain­able top-line growth in health­care

2021 saw a record $600B in healthcare M&A activity. In 2022, there is an anticipated slowdown in activity, however, M&A prospects remain strong in the medium to long-term. What are future growth drivers for the healthcare sector? Where might we see innovations that drive M&A? RBC’s Andrew Callaway, Global Head, Healthcare Investment Banking discusses with Vito Sperduto, Global Co-Head, M&A.

15 LGBTQ lead­ers in bio­phar­ma; Paul Stof­fels’ Gala­pa­gos re­vamp; As­traZeneca catch­es up in AT­TR; 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.

A return to in-person conferences also marks a return to on-the-ground reporting. My colleagues Beth Synder Bulik and Nicole DeFeudis were on-site at Cannes Lions, bringing live coverage of pharma’s presence at the ad festival — accompanied by photos from Clara Bui, our virtual producer, that bring you right to the scene. You can find a recap (and links to all the stories) below.

Endpoints News

Keep reading Endpoints with a free subscription

Unlock this story instantly and join 144,300+ biopharma pros reading Endpoints daily — and it's free.

David Loew (Ipsen)

Ipsen snags an ap­proved can­cer drug in $247M M&A deal as an­oth­er bat­tered biotech sells cheap

You can add Paris-based Ipsen to the list of discount buyers patrolling the penny stock pack for a cheap M&A deal.

The French biotech, which has had plenty of its own problems to grapple with, has swooped in to buy Epizyme $EPZM for $247 million in cash and a CVR with milestones attached to it. Epizyme shareholders, who had to suffer through a painfully soft launch of their EZH2a inhibitor cancer drug Tazverik, will get $1.45 per share along with a $1 CVR tied to achieving $250 million in sales from the drug over four consecutive quarters as well as an OK for second-line follicular lymphoma by 1 Jan. 2028.

Endpoints News

Keep reading Endpoints with a free subscription

Unlock this story instantly and join 144,300+ biopharma pros reading Endpoints daily — and it's free.

AstraZeneca's new Evusheld direct to consumer campaign aims to reach more immunocompromised patients.

As­traZeneca de­buts first con­sumer cam­paign for its Covid-19 pro­phy­lac­tic Evusheld — and a first for EUA drugs

AstraZeneca’s first consumer ad for Evusheld is also a first for drugs that have been granted emergency use authorizations during the pandemic.

The first DTC ad for a medicine under emergency approval, the Evusheld campaign launching this week aims to raise awareness among immunocompromised patients — and spur more use.

Evusheld nabbed emergency authorization in December, however, despite millions of immunocompromised people looking for a solution and now more widespread availability of the drug.

Endpoints News

Keep reading Endpoints with a free subscription

Unlock this story instantly and join 144,300+ biopharma pros reading Endpoints daily — and it's free.

Joe Papa (Ryan Remiorz/The Canadian Press via AP, File)

Joe Pa­pa re­signs as chair of Bausch Health as bil­lion­aire John Paul­son takes over

Joe Papa, chair of Bausch Health, officially resigned on Thursday and the board appointed billionaire hedge fund manager John Paulson as the new chair, effective immediately.

The specialty pharma company sought to make clear that Papa’s abrupt departure “was not due to any dispute or disagreement with the Company, its management or the Board on any matter relating to the Company’s operations, policies or practices.”

Endpoints News

Keep reading Endpoints with a free subscription

Unlock this story instantly and join 144,300+ biopharma pros reading Endpoints daily — and it's free.

Yong Dai, Frontera Therapeutics CEO

Scoop: Lit­tle-known Or­biMed-backed biotech clos­es $160M round to start gene ther­a­py tri­al

Frontera Therapeutics, a China and US biotech, has closed a $160 million Series B and received regulatory clearance to test its first gene therapy stateside, Endpoints News has learned.

Led by the largest shareholder, OrbiMed, the biotech has secured $195 million total since its September 2019 founding, according to an email reviewed by Endpoints. The lead AAV gene therapy program is for an undisclosed rare eye disease, according to the source.

Endpoints News

Keep reading Endpoints with a free subscription

Unlock this story instantly and join 144,300+ biopharma pros reading Endpoints daily — and it's free.

Spanish Prime Minister Pédro Sanchez and European Commission President Ursula von der Leyen (AP Photo/Geert Vanden Wijngaert)

EU to launch vac­cine de­vel­op­ment and man­u­fac­tur­ing part­ner­ship with Latin Amer­i­can and Caribbean coun­tries

While European companies, including BioNTech, are focused on increasing vaccine access to African countries by setting up vaccine manufacturing facilities, the European Union is looking westward to Latin America and the Caribbean.

Speaking at a press conference with Spanish Prime Minister Pédro Sanchez, EU Commission president Ursula von der Leyen said that the EU is launching a new initiative for vaccines and medicines manufacturing in Latin America, to get drugs to Latin America and the Caribbean faster.

DEM BioPharma CEO David Donabedian (L) and executive chair Jan Skvarka

Long­wood sets an­oth­er 'don't eat me' biotech in­to gear with help of for­mer Tril­li­um CEO Jan Skvar­ka

Jonathan Weissman and team are out with a cancer-fighting biotech riding the appetite for those so-called “don’t eat me” and “eat me” signals.

The scientific co-founder — alongside fellow Whitehead Institute colleague Kipp Weiskopf and Stanford biologist Michael Bassik — has launched DEM BioPharma with incubator Longwood Fund and a crop of other investors.

In all, the nascent, 10-employee biotech has $70 million to bankroll hematology- and solid tumor-based programs, including a lead asset that could enter human trials in two to three years, CEO David Donabedian told Endpoints News.

Endpoints News

Keep reading Endpoints with a free subscription

Unlock this story instantly and join 144,300+ biopharma pros reading Endpoints daily — and it's free.

GSK says its drug for chron­ic hep B could ‘lead to a func­tion­al cure’ — but will it be alone or in com­bi­na­tion?

GSK, newly branded and soon-to-be demerged, shared interim results from its Phase II trial on its chronic hepatitis B treatment, one that it says has the “potential to lead to a functional cure.”

At a presentation at the EASL International Liver Congress, GSK shared that in around 450 patients who received its hep B drug bepirovirsen for 24 weeks, just under 30% had hepatitis B surface antigen and viral DNA levels that were too low to detect.