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BIO:ON Insight EN #19 Β· Oct 6, 2026 Β· China Sourcing Β· US Pricing Model Β· Korean Biosimilars Discovery in China, manufacturing in Korea,
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Last issue was one company on three fronts. This week the picture flips: it's about which country plays which role. Novartis is buying next-generation drug candidates from China, Samsung Bioepis develops and manufactures while Teva sells, and the US has just decided to benchmark Medicare drug prices against other countries. Who discovers, who manufactures, who sets the price: the map of the biotech value chain is quietly being redrawn. The question for you is where on it you want to stand.
β Editor Β· MSc Biotechnology & Pharmaceutical Management
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π€ Word of the Week
International reference pricing
a.k.a. most-favoured-nation (MFN) pricing, the idea behind CMS's GLOBE model (Story 2)
Setting a drug's price by asking "what do other countries pay for this?" is called international reference pricing. Many European countries, and Korea, already do some version of it. The US has been the outlier: manufacturers set the price and insurers or the government negotiate afterwards, which made it the most expensive market in the world. Now CMS has said that for Part B drugs, the ones administered by a doctor or in a hospital, it will use prices from economically comparable countries as the cost benchmark.
Until now β "we set our own price" πΊπΈ
Manufacturers set the US price and payers negotiated afterwards. What other countries paid had no direct effect on what the US paid.
GLOBE β "what do other countries pay?" π
For Part B drugs, comparison countries' prices become the cost benchmark. A low price abroad can pull the US benchmark down, so where and when you launch starts to affect US revenue.
π° This Week's Top 3 Stories
Novartis Bets Up to $7.8B on Abogen's mRNA "In-Body" T-Cell Engager for Autoimmune Disease
Fierce Biotech Β· Novartis (NYSE: NVS) Γ Abogen Biosciences | Oct 2, 2026
Key Facts
Novartis is paying China-based Abogen Biosciences $575 million upfront and up to $7.2 billion in milestones for global rights to ABO2203. The drug is an mRNA-encoded CD19xCD3 T-cell engager delivered in lipid nanoparticles, so the patient's own body makes the engager after injection. Its lead indication is immune thrombocytopenia (ITP), and it is also being tested in B-cell non-Hodgkin lymphoma. The deal includes an option on Abogen's next-generation RNA platform, so Novartis is buying a way into a technology as well as one asset.
Plain-English Breakdown π§©
CAR-T means taking a patient's cells out, engineering them and putting them back, with lymphodepleting chemotherapy and a hospital stay first. ABO2203 aims to deplete B cells with an injection, which could be given in an outpatient setting and possibly at lower cost. The timing stands out: Novartis recently paused an autoimmune CAR-T programme after three deaths (we covered it in #15), so this reads as a move to a lower-risk way into the same market. It's still early-stage, though, so efficacy and safety have yet to be proven.
π Global Lens
China is again the source of a next-generation modality, the second big China deal in two issues after Lilly and InnoCare. Other hubs such as Korea, Japan and Europe have to decide whether to compete for the same early-stage assets or on other strengths like manufacturing and clinical execution. Regulators including the FDA will watch the early safety data closely, because an engager produced inside the body is a new kind of product.
Why it matters for your career: BD teams need people who can value an option on a platform, not just a single asset, and scientists who understand mRNA-LNP delivery and T-cell engagers will be in demand.
π After pausing a CAR-T programme over deaths, Novartis has switched to a less frightening way into the same market. β Fierce Biotech summary
CMS Locks In "GLOBE," Bringing Most-Favored-Nation Pricing to Medicare Part B
Fierce Healthcare Β· CMS | Sep 30, 2026
Key Facts
CMS finalised the Global Benchmark for Efficient Drug Pricing (GLOBE) Model, which sets cost benchmarks for physician-administered Part B drugs using prices from economically comparable countries. It runs from January 1, 2027 to March 31, 2032 and covers about 25% of traditional Medicare beneficiaries in randomly selected regions. Patients there should see lower out-of-pocket coinsurance from April 1, 2027. After public comments, CMS excluded biosimilars, reference biologics once a biosimilar launches, orphan drugs, plasma-derived products and some cell and gene therapies.
Plain-English Breakdown π§©
In plain terms, the US now formally prices against international benchmarks. If a company launches in a lower-priced market like the UK or Korea at a low price, that price can feed back into the US benchmark. So launch sequencing and list-price corridors stop being an ex-US sales question and become a US revenue decision. The exemptions also give orphan, biosimilar and advanced-therapy portfolios a clear advantage within Part B.
π Global Lens
GLOBE is a US model, but it reaches every market it references. Prices agreed with payers such as NICE in England or in Korea's HIRA-linked system can now affect US benchmarks, which may delay or reshape launches in lower-priced markets like the UK and Korea. Companies will have to plan country by country, with Washington in the room.
Why it matters for your career: Global pricing, market access and launch-strategy teams will need people who can model how a foreign price flows into US revenue, and who can connect payer policy to commercial strategy.
π Foreign prices now shape the US benchmark, so launch order has become revenue strategy. β Fierce Healthcare summary
Teva and Samsung Bioepis Expand Their Alliance with Six New Biosimilars
Fierce Pharma Β· Teva (NYSE: TEVA) Γ Samsung Bioepis | Oct 2, 2026
Key Facts
Teva and Korea's Samsung Bioepis agreed to co-develop and commercialise up to six biosimilar candidates; financial terms were not disclosed. Two candidates reference AstraZeneca's Fasenra and one references Novartis's Ilaris. Samsung Bioepis will handle development, regulatory work and manufacturing, while Teva commercialises in the US, Europe and Canada, with an option to add other territories. It is the third deal between the companies in 2026, after Epysqli (a Soliris biosimilar) in the US in January and Opuviz (an Eylea biosimilar) in Canada this summer.
Plain-English Breakdown π§©
As major biologics lose patent protection from the late 2020s into the early 2030s, more biosimilar competition should lower prices for severe asthma and rare autoinflammatory diseases and widen access to them. What's interesting is that the split of roles is hardening: a Korean company develops and manufactures, a Western partner sells. It also fits Teva CEO Richard Francis's "Pivot to Growth" strategy, a big US commercial platform that partners for development rather than funding R&D itself.
π Global Lens
Samsung Bioepis is the developer and manufacturer for markets reached through Teva's commercial network in the US, Europe and Canada. As patents on major biologics expire, payers in all those markets will be looking for cheaper biosimilars, and both the FDA and the EMA have established biosimilar pathways. For other Asian manufacturers, this is a template for moving up the value chain.
Why it matters for your career: Biosimilar programmes need analytical, CMC and regulatory people, plus alliance managers who can run a partnership where one company builds and another sells.
π Korea builds, the West sells, and this year the pattern has now been set three times. β Fierce Pharma summary
π¬ This Week's Deep Dive
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π‘ Editor's Insight
π Numbers of the Week
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$7.8B |
Maximum Novartis could pay Abogen $575M upfront plus $7.2B in milestones, including an option on Abogen's next-generation RNA platform. |
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25% |
Share of traditional Medicare beneficiaries covered by GLOBE In randomly selected regions, from January 2027 to March 2032. Patients' coinsurance changes from April 2027. |
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6 |
Biosimilar candidates Teva and Samsung Bioepis will co-develop The third deal between the two in 2026, and a sign the Korea-builds, West-sells split is hardening. |
π 3 Stocks That Moved This Week
Direction and catalyst, sketched β not exact prices. Check a real chart for that.
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Teva Pharmaceutical NYSE: TEVA |
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β² Up |
Shares rose on the expanded alliance with Samsung Bioepis, which reinforces Teva's "Pivot to Growth" idea of a big US sales platform plus a partner's development and manufacturing. Hiring signal: alliance management and biosimilar commercial teams are likely to grow as six candidates move forward. (Directional sketch.)
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Novartis NYSE: NVS |
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β Flat |
Shares barely reacted to the $7.8B licensing deal; for a company this size it's a rounding error. The market seems more interested in ABO2203's early clinical data than the headline. Hiring signal: expect immunology BD and mRNA or LNP science roles to be worth watching. (Directional sketch.)
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Merck NYSE: MRK |
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β½ Down |
Shares slipped as GLOBE's confirmation revived worries about long-term price pressure on big Part B products. How far exemptions and the real effect go is still to be seen. (Directional sketch.)
π Why this pattern
This week, who sits inside the price-benchmark zone decided the reaction: Teva rose on a partnership that adds to its growth story, Novartis stayed calm on a big deal, and Merck, with large Part B products, slipped. (All directional sketches β check a real chart for exact prices.)
π― Roles to Watch This Week
Teams worth watching based on this issue's news β not live job postings, so check each company's careers page for what's actually open.
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Novartis β Business Development / Licensing (immunology, RNA) Why now: buying a drug plus an option on a platform needs people who can value the option, structure milestones and manage a cross-border alliance. Look under "Business Development & Licensing" on Novartis's careers page, and mRNA/LNP research roles on the science side. |
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Global Pricing & Market Access (companies with Part B portfolios) Why now: GLOBE makes foreign list prices a US revenue input, so pricing teams need people who can model launch-sequence scenarios. Look under "Global Pricing," "Market Access" or "Pricing & Reimbursement" at big pharma. |
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Samsung Bioepis / Teva β Biosimilar Development and Alliance Management Why now: six candidates across two companies need analytical, CMC and regulatory work on one side and alliance management on the other. Check Samsung Bioepis's careers page for development roles and Teva's for alliance and biosimilar commercial roles. |
ποΈ Dates to Watch
| When / Event | Why It Matters |
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Q4 2026 β 2027 (expected) Novartis β first ABO2203 clinical data; decision on Abogen's RNA platform option |
Early ITP data will show whether this deal turns out to be an expensive bet or a well-chosen one. |
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Jan 1 and Apr 1, 2027 CMS β GLOBE starts (Jan 1); patient coinsurance changes in selected regions (Apr 1) |
The first point to see whether launch order and pricing really change, and whether launches in lower-priced markets like the UK and Korea start slipping. |
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2027 onwards (expected) Teva Γ Samsung Bioepis β six candidates become more concrete; first trial starts |
Terms are undisclosed, so whether the deal size comes out and how fast development moves are what to watch. |
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Check exact dates before booking BIO-Europe (November) and the ASH Annual Meeting (December) |
Relevant to this issue's BD, immune-cell and lymphoma themes; some offer discounted student passes and are among the cheapest ways to network into BD, clinical or research roles. Confirm each year's dates first. |
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π Sources
β Novartis bets up to $7.8B on Abogen's mRNA in-body T-cell engager (Fierce Biotech, Oct 2, 2026) β‘ CMS locks in GLOBE, bringing most-favored-nation pricing to Medicare Part B (Fierce Healthcare, Sep 30, 2026) β’ Teva and Samsung Bioepis expand their alliance with six new biosimilars (Fierce Pharma, Oct 2, 2026)
Global biotech & pharma news, translated into career signal β π Read on the web Β· past issues archive β bioon-website.vercel.app Β© 2026 BIO:ON Insight Β· Unsubscribe here. |