PERSON DIRECTORY
Brian Skorney
Brian Skorney appears in 25 indexed conversations across Biotech Hangout. This directory brings every appearance, source, TL;DR, digest, and transcript into one searchable feed.
Episode 184 - May 29, 2026
Chris GarabedianBrian SkorneyGraig SuvannavejhJason Kelly
Biotech capital markets are recovering: Cardigan is the 11th 2026 IPO filing, while Endpoints sentiment reached 96 and finance/investment stakeholders reached 120.Ginkgo’s cell-engineering thesis, Lilly’s up-to-$3.8B vaccine buying, Apogee’s up-to-$1.3B financing, and ASCO’s RESOLUTE 302 readout leave regulation and tolerability to monitor.
Episode 134 - March 14, 2025
Grace ColónJosh SchimmerEric SchmidtBrian Skorney
Novo’s CagriSema delivered 12.6% placebo-adjusted weight loss in REDEFINE 2, broadly in line with Zepbound, but the stock fell roughly 8–10%.Policy risks include MFN pricing, tariffs and vaccine trust, while PBM reform, IRA fixes and the tax bill offer upside; a report expected the week of April 7 could be a catalyst.
Episode 171 - January 30, 2026
Josh SchimmerSam FazeliBrian SkorneyYaron WerberJohn Crowley
BIO CEO John Crowley says rising US trial costs and regulatory uncertainty make capital flowing to China “perfectly rational.”His FDA prescription—stability, consistency, transparency, and modernization—puts “the next 6 months” in focus.MFN codification could be “devastating” and “unmanageable” before Section 232 action due by the last week of March, while ReGenix’s PLAG1 integration tests AAV safety.
Episode 165 - December 5, 2025
Josh SchimmerBrian SkorneyPaul MatteisGraig Suvannavejh
Biotech enters 2026 on launches rather than dreams, with limited pricing pressure, more M&A, XBI still cheap over five years, and rates the key macro risk.IPO expectations range from 15 to roughly 50 or more, but preclinical FOMO remains a crash signal; meanwhile, FDA turnover makes uniQure’s reversal a test of whether prespecified agreements still carry weight, while Capricor and Praxis offer near-term approval catalysts.
Episode 162 - November 7, 2025
Graig SuvannavejhPaul MatteisBrian SkorneyYaron WerberChris GarabedianAdam Feuerstein
George Tidmarsh’s CBER departure and UniQure’s rejected filing after FDA alignment expose a widening gap between flexible guidance and unpredictable execution.UniQure reported 80% disease slowing at two years and 75% at three years for high dose, while Sarepta’s failed ESSENCE study and December’s Stoke meeting will test evidence standards and early-filing appetite.
Episode 150 - August 1, 2025
Daphne ZoharJosh SchimmerBrian SkorneyPaul MatteisSam FazeliBrad LoncarMatt Gline
Trump’s letters to 17 pharma CEOs make MFN a risk, though no statutory authority was cited and implementation remains discounted.Medicaid and direct-to-consumer pricing may be easier; tougher IRA negotiations remain possible around September 29.GSK–Hengrui’s Phase 1 options and China’s 30% share of global trial starts sharpen outsourcing concerns; AHEAD’s 85%–90% screen-failure rate remains unresolved.
Episode 149 - July 25, 2025
Eric SchmidtPaul MatteisSam FazeliBrian Skorney
Elevidys escalated from restructuring to an FDA-requested, then accepted, full shipment halt after a third death, exposing regulatory, disclosure, debt, and political risks for Sarepta.Replimune’s RP1 delivered low-30s ORR with roughly half complete responses versus single-digit standard-of-care rates but received a CRL over its single-arm study, while Tidmarsh’s industry background and shifting FDA signals leave approval flexibility and small-biotech capital costs unresolved.






