Held by
0
portfolios on TandT
Bookmarked by
0
users
Avg position size
—
of holders' portfolios
13F filers
3
institutions
Market cap
$1.1T
891M shares
52-week range
$655.10 – $1,249.45
93% from low
Sector
PHARMACEUTICAL PREPARATIONS
Exchange
NYSE
CS
Eli Lilly is a drug firm with a focus on neuroscience, cardiometabolic, cancer, and immunology. Lilly's key products include Verzenio and Jaypirca for cancer; Mounjaro, Zepbound, Foundayo, Jardiance, Trulicity, Humalog, and Humulin for cardiometabolic; and Taltz and Olumiant for immunology.
www.lilly.comNo one on the platform currently holds LLY.
| Institution | Shares | Reported |
|---|---|---|
| The Baupost Groupas of 2024-12-31 | 782,860 | $604.4M |
| Renaissance Technologiesas of 2026-03-31 | 71,788 | $66.0M |
| Ex-date | Per share | Pay date |
|---|---|---|
| 2026-08-14 | $1.7300 | 2026-09-10 |
| 2026-05-15 | $1.7300 | 2026-06-10 |
| 2026-02-13 | $1.7300 | 2026-03-10 |
| 2025-11-14 | $1.5000 | 2025-12-10 |
| 2025-08-15 | $1.5000 | 2025-09-10 |
| 2025-05-16 | $1.5000 | 2025-06-10 |
| 2025-02-14 | $1.5000 | 2025-03-10 |
| 2024-11-15 | $1.3000 | 2024-12-10 |
| 2024-08-15 | $1.3000 | 2024-09-10 |
| 2024-05-15 | $1.3000 | 2024-06-10 |
No one on the platform has traded LLY yet.
| 70,812 |
| $65.1M |
| 2024-02-14 | $1.3000 | 2024-03-08 |
| 2023-11-14 | $1.1300 | 2023-12-08 |
| Year | Est. revenue | Growth | Est. EPS | EPS range | Fwd P/E | # Analysts |
|---|---|---|---|---|---|---|
| 2026 | $86.8B | +35.9% | $36.13 | $33.86–$38.73 | 33.5× | 12 |
| 2027 | $100.4B | +15.8% | $46.17 | $41.47–$48.52 | 26.2× | 13 |
| 2028 | $112.0B | +11.5% | $53.03 | $47.49–$60.65 | 22.8× | 6 |
| 2029 | $121.8B | +8.8% | $59.19 | $54.89–$63.98 | 20.4× | 3 |
Forward consensus · growth is YoY vs the prior fiscal-year estimate · Fwd P/E at the current price · source: Financial Modeling Prep
Beat consensus in 7 of the last 8 reported quarters
| Reported | Est. EPS | Actual | Surprise |
|---|---|---|---|
| 2026-08-05 | $6.40 | $8.38 | +30.9% |
| 2026-04-30 | $6.97 | $8.55 | +22.7% |
| 2026-02-04 | $6.91 | $7.54 | +9.1% |
| 2025-10-30 | $5.69 | $7.02 | +23.4% |
| 2025-08-07 | $5.60 | $6.31 | +12.7% |
| 2025-05-01 | $3.26 | $3.34 | +2.5% |
| 2025-02-06 | $5.03 | $5.32 | +5.8% |
| 2024-10-30 | $1.47 |
| $1.18 |
| -19.7% |
| $171.5B |
| — |
| JNJJohnson & Johnson | $262.08 | +0.47% | $631.6B | — |
| MRKMerck & Co., Inc. | $135.55 | +1.98% | $334.8B | — |
Source: Financial Modeling Prep · peers by sector/industry
Click to see transaction details on SEC.gov. Form 4s cover trades by officers, directors, and 10%+ owners, due within 2 business days of the trade.
For any #microcap #pharma #stock with a #new #FDAapproval, is there an #average #number of #quarters to #switch from -#negative to #positive #EPS? $BRK.B $MCK $LLY $MRK
View on StockTwits ↗$LEXX $LLY $NVO $RANI $VKTX They tryna everything they can to hide the facts but it’s too late 🧨 Lexaria is blowing up 🔥
View on StockTwits ↗$NVO $LLY Part 3 out of 3 15. What this means specifically for Novo Nordisk The strongest Novo bull thesis is therefore not: “Novo will beat Lilly and regain every point of market share.” That would be unnecessarily demanding. A much more powerful thesis is: Novo does not need to win the entire GLP-1 market. It needs to remain one of the dominant platforms while the market itself becomes dramatically larger. Consider again: A company with 40% of a 100-unit market has 40 units. A company with only 25% of a 400-unit market has 100 units. It lost: 15 percentage points of market share while increasing absolute volume: 150%. That is why the critical Novo variables over the coming quarters should be: absolute prescription growth, new-to-GLP-1 starts, oral-market expansion, international patient growth, Medicare adoption, payer access, persistence, and total obesity-market volume. Not simply: “Did Lilly gain another percentage point?” In 2025 the global branded GLP-1 obesity market already expanded 104% by volume, demonstrating that denominator expansion is not theoretical. (Novo Nordisk Annual Report) And Wegovy pill’s early launch provides another particularly important signal: Novo reported that the majority of new prescriptions were going to people new to GLP-1 treatment. (Novo Nordisk) That is precisely the evidence one would expect to see if a second adoption wave were beginning. ⸻ Final bull thesis The obesity-treatment opportunity should be viewed not as a finite 100-patient market in which Lilly can grow only by taking Novo’s patients, but as an enormous, expanding chronic-disease population in which the treated denominator itself may multiply. Nearly 900 million adults already live with obesity globally, billions live with excess weight, and prevalence continues rising, while actual branded pharmacological penetration remains small relative to the potential population. The first GLP-1 wave demonstrated extraordinary efficacy and created consumer awareness, but adoption was constrained by injections, high prices, insurance exclusions, prior authorization, manufacturing shortages and limited geographic availability. Beginning in 2026, many of those constraints are weakening simultaneously: effective oral GLP-1s have launched, entry-level self-pay pricing has fallen toward $149 per month, Medicare has created a $50-per-month pathway for eligible beneficiaries, commercial coverage is widening, direct-to-patient distribution is expanding, manufacturing capacity is increasing and oral Wegovy is already bringing previously untreated people into the category. The investment implication is that market-share analysis alone can dramatically understate the opportunity. Novo could lose relative share to Lilly while still adding millions of patients and materially increasing absolute obesity-drug volume if the overall treated market grows faster than its share declines. Lilly can grow without destroying Novo; Novo can grow without defeating Lilly. The true bull case is therefore not that one company wins a zero-sum obesity war. It is that obesity pharmacotherapy progresses from a constrained specialty market into a routine global chronic-disease treatment category, causing tens of millions of currently untreated people to become recurring pharmaceutical patients. If that transition occurs, 2022–2025 will ultimately look less like the GLP-1 boom itself and more like the first chapter of a substantially larger adoption curve. Not financial advice. All personal opinions. Long nvo
View on StockTwits ↗$NVO $LLY Part 2 out of 3 7. Medicare represents another enormous barrier beginning to crack Until recently, lack of broad Medicare coverage created a particularly large hole in obesity treatment among older Americans. That changed on July 1, 2026, when CMS launched the Medicare GLP-1 Bridge. Eligible Medicare Part D beneficiaries can receive certain obesity GLP-1 medicines—including Wegovy formulations, Foundayo and qualifying Zepbound formulations—for a $50 monthly copayment, subject to eligibility and prior authorization. The program currently runs through December 31, 2027. (Centers for Medicare & Medicaid Services) This program has existed for only about six weeks as of August 13, 2026. Therefore it would be premature to judge its long-run patient-volume contribution from initial uptake. There is physician education. There is patient awareness. There is prior authorization. There are pharmacy processes. There are follow-up appointments. There is normal healthcare-system inertia. A newly created reimbursement pathway does not immediately convert every eligible patient. Adoption propagates. That is why 2027 may look very different from July or August 2026. ⸻ 8. Commercial insurance is moving as well The same process is occurring outside Medicare. Lilly announced in May 2026 that the three largest U.S. pharmacy benefit managers would cover its obesity portfolio under their respective arrangements, expanding access to Foundayo and Zepbound for millions of commercially insured Americans. (Lilly Investor Relations) Coverage is still far from universal. Medicaid obesity coverage remains restricted in many states, and payers remain extremely concerned about the aggregate cost of treating such a large population. (KFF) But that actually reinforces the central thesis. The market has reached its existing scale despite substantial access restrictions. Therefore additional payer penetration represents incremental upside rather than something already completely exhausted. ⸻ 9. International expansion provides another denominator The GLP-1 story is often discussed as though America is the market. It isn’t. Novo had made Wegovy available in 52 countries by the end of 2025, versus only 17 in 2024, and continued planning additional rollouts. (Novo Nordisk Annual Report) In July 2026 the European Commission approved Wegovy pill for weight management in the EU. (Novo Nordisk) So the same sequence that happened in America can potentially occur across: Europe, Asia, Latin America, the Middle East, and eventually much larger portions of the developing world. The global obesity burden also continues shifting toward developing economies. The GBD study projects particularly large increases in overweight and obesity populations in Asia and sub-Saharan Africa through 2050. (PubMed Central (PMC)) The U.S. may therefore be less the endpoint than the proof of concept. ⸻ 10. Why hasn’t everyone already demanded these medicines if obesity is dangerous? Because chronic diseases do not generate the same psychological urgency as acute diseases. If a doctor tells someone: “Without this medicine you may die tonight,” adherence is likely to be extraordinarily high. Obesity usually works differently. Its major consequences—including type 2 diabetes and cardiovascular disease—often develop over years or decades. WHO classifies obesity as a chronic, relapsing disease and links excess weight to substantial long-term health consequences. (World Health Organization) A person can therefore wake up at 35, feel relatively normal and postpone treatment. Then postpone it again at 36. And again at 37. Human beings heavily discount future risk. That means medical necessity alone is insufficient to produce instant adoption. The treatment must also become: easy enough, cheap enough, safe enough, socially accepted enough, accessible enough, and compelling enough to convert latent demand into actual prescriptions. That is what the next stage of the industry is solving. ⸻ 11. Better drugs can expand the market again Today’s medicines are unlikely to represent the final form of obesity treatment. Novo now has multiple formulations of semaglutide plus development programs including CagriSema and zenagamtide/amycretin. Lilly has Zepbound, Foundayo and retatrutide. Lilly’s Phase 3 TRIUMPH-1 study reported average weight reduction of up to 28.3% at 80 weeks with retatrutide in adults with obesity. (Lilly Investor Relations) Novo’s approved higher-dose 7.2 mg Wegovy has demonstrated weight reduction around 20%+ in Phase 3 testing, depending on the analysis population. (Novo Nordisk) Future generations could compete on far more than raw weight reduction: maintenance, cardiovascular outcomes, muscle preservation, tolerability, dosing frequency, oral convenience, specific comorbidities, and personalization. Every meaningful improvement can convert another group of patients who previously said: “Not for me.” That means product innovation doesn’t necessarily just redistribute existing GLP-1 patients. It can expand the category. ⸻ 12. Obesity treatment may eventually become segmented rather than winner-take-all Investors frequently model Novo and Lilly like Coke versus Pepsi. But medicine generally doesn’t work that way. Different patients have different priorities. One may want maximum weight loss. Another may prioritize cardiovascular evidence. Another refuses injections. Another needs the cheapest option. Another experiences intolerable GI effects from one molecule. Another may need diabetes control. Another may be interested primarily in sleep apnea, MASH or another obesity-associated condition. Even Novo CEO Mike Doustdar argued in August 2026 that obesity treatment is unlikely to become a winner-take-all market because patients will increasingly segment among different medicines. Reuters reported that Wegovy pill currently holds roughly 90% of the oral GLP-1 market, according to Novo, even as Lilly remains extremely strong in injectable obesity therapy. (Reuters) That is exactly what segmentation looks like. Novo doesn’t necessarily have to beat Lilly everywhere. Lilly doesn’t necessarily have to destroy Novo. They can dominate different portions of an enormous expanding market. ⸻ 13. The second-wave mechanism This is therefore the mechanism I would watch from 2026 through approximately 2028: More obesity ↓ More medically eligible people ↓ Greater awareness of GLP-1 treatment ↓ Pills remove injection resistance ↓ Lower cash prices remove affordability resistance ↓ Medicare and commercial coverage remove reimbursement resistance ↓ Telehealth/direct channels reduce physician-access friction ↓ Manufacturing expansion removes supply constraints ↓ International approvals expand geography ↓ Better next-generation drugs expand patient choice ↓ More first-time GLP-1 patients ↓ Larger installed treatment population ↓ Refills + new starts compound patient volume ↓ A much larger global obesity pharmaceutical market This is what I mean by the second wave. Wave One was: “These drugs actually work.” Wave Two is: “These drugs are becoming accessible enough for tens of millions more people to actually use them.” And Wave Three may eventually become: “Obesity pharmacotherapy is simply routine medicine.” ⸻ 14. The crucial difference between a finite market and a compounding patient market Imagine a company selling refrigerators. Someone buys one. They probably don’t buy another one next month. The company must continuously find replacement customers. Chronic medicine behaves differently. A successfully treated patient may continue receiving therapy repeatedly, while additional patients begin treatment. Conceptually: **Existing retained patients * new patient starts − discontinuations = next period’s patient base.** If new starts exceed discontinuations, the installed treatment population grows. Then new patients are added to an increasingly large base. That produces a potentially powerful volume-compounding mechanism. The challenge is persistence: real-world GLP-1 discontinuation remains meaningful, and cost and side effects are important reasons people stop therapy. KFF’s polling specifically identified both affordability and adverse effects as leading discontinuation reasons. (KFF) But that also identifies another source of future upside. If affordability improves and future drugs improve tolerability or maintenance, retention can rise. Then the industry benefits twice: more people start and more people remain on therapy. Not financial advice, all personal opinions. Long nvo.
$NVO $LLY all right boys let me get everyone’s attention again, I will explain why you don’t bet against Lily or NVO. You either buy both or buy one. Never short glp market. It’s terrifying for shorties. Part 1 out of 3 The Second Wave of Obesity Medicine — The Bull Thesis Core thesis The central bull thesis for the obesity-drug industry is that investors may be treating Novo Nordisk and Eli Lilly as if they are fighting over a relatively fixed pool of patients, when in reality they are competing inside one of the largest, most underpenetrated, expanding chronic-disease markets in medicine. The first GLP-1 wave proved that pharmacological weight loss works. The second wave—likely unfolding from 2026 through the remainder of the decade—is about removing the barriers that prevented hundreds of millions of eligible people from becoming patients: price, insurance coverage, injections, physician access, manufacturing capacity, geographic availability and treatment choice. If those barriers continue falling, the dominant source of future growth does not have to be Novo stealing patients from Lilly or Lilly stealing patients from Novo. It can be millions of previously untreated people entering the market for the first time. That distinction changes the entire investment thesis. ⸻ 1. Start with the denominator: the potential population is enormous This is not a disease affecting ten or twenty million people. WHO estimates that in 2022 approximately 2.5 billion adults were overweight, including more than 890 million adults living with obesity. Worldwide adult obesity prevalence has more than doubled since 1990. (World Health Organization) And the denominator does not appear to be shrinking. A major Global Burden of Disease forecasting study published in The Lancet projects that, if historical trends continue, approximately 3.8 billion adults aged 25+ could have overweight or obesity by 2050, including roughly 1.95 billion living with obesity. (PubMed Central (PMC)) That means the obesity pharmaceutical industry is not necessarily chasing a patient population that will eventually be exhausted. The potential pool is continually replenished by: new people developing obesity, younger populations aging into treatment, patients becoming medically eligible, people receiving an obesity diagnosis for the first time, new countries gaining access, insurance expanding coverage, and people who previously refused treatment changing their minds as medicines become cheaper, easier and better. Therefore, the market has two potential growth engines simultaneously: growth of the underlying eligible population and growth in the percentage of that population receiving treatment. The second factor could be much more powerful than the first. ⸻ 2. Treatment penetration remains tiny relative to the medical need Consider one number. Novo Nordisk reported treating approximately 3.6 million people globally with obesity in 2025. Its obesity business nevertheless generated DKK 82.3 billion of revenue and grew 31% at constant exchange rates. (Novo Nordisk Annual Report) Compare: 3.6 million Novo obesity patients with ~890 million adults already living with obesity globally. This is not saying only 3.6 million people globally receive obesity medication—Lilly, other drugs and other channels obviously add additional patients. The important point is the order of magnitude. Novo can operate an enormous obesity franchise while reaching only a tiny fraction of the global disease population. That is characteristic of an underpenetrated market, not a mature one. And the branded GLP-1 obesity market is still expanding extraordinarily quickly. Novo reported that global branded GLP-1 obesity-market volume increased 104% during 2025. (Novo Nordisk Annual Report) That is one of the strongest pieces of evidence for the thesis. The companies are not merely rearranging existing patients. The category itself is expanding. ⸻ 3. This is why market share can be extremely misleading Suppose there are initially 100 treated obesity patients. Lilly has: 55 Novo has: 40 Others have: 5 Now imagine that five years later the treated market expands from 100 patients to 250 patients. And Novo actually loses market share from 40% to only 30%. Novo would then have: 30% × 250 = 75 patients. Its market share fell: 40% → 30% but its absolute patients increased: 40 → 75 or roughly 88%. That is the mathematical insight that matters. Losing share does not necessarily mean losing patients. If the denominator expands sufficiently quickly, both competitors can become dramatically larger businesses while fighting each other intensely. This is why thinking about obesity as: “Will Lilly beat Novo?” can lead investors to the wrong conclusion. A better question is: “How quickly will the number of treated obesity patients expand?” Lilly could remain the injectable leader. Novo could lose some injectable share. And yet Novo’s total obesity volume could still grow substantially if oral drugs, international expansion, Medicare, self-pay channels and greater medical adoption create millions of incremental patients. That is the bull case. ⸻ 4. The first wave proved the medicine works; the second wave removes friction The first great GLP-1 adoption wave occurred roughly from 2021 through 2025. Wegovy, Ozempic, Mounjaro and Zepbound transformed expectations about pharmacological weight management. But there was an enormous problem. The drugs could work extremely well medically while still being difficult to obtain commercially. A potential patient had to confront some combination of: high prices insurance exclusions prior authorization doctor appointments injections supply shortages limited manufacturing limited international availability side effects uncertainty about long-term therapy Every friction point reduces the conversion rate from: “I would like obesity treatment” to “I am actually taking obesity medication every month.” KFF’s polling illustrates this gap. Among Americans who reported having been diagnosed with overweight or obesity, 23% said they were currently taking a GLP-1 in late 2025. Yet among diagnosed overweight/obese adults who weren’t currently using one, 43% said they were interested in using a GLP-1 for weight loss. (KFF) There is therefore a substantial difference between interest and actual treatment. Why? Cost is one obvious explanation. KFF found that 56% of people who had used GLP-1 medicines reported difficulty affording them, while cost was among the most common reasons people discontinued therapy. (KFF) That is exactly what a bottleneck looks like. It means existing sales don’t necessarily measure underlying medical demand. They measure medical demand after applying all the current obstacles to access. ⸻ 5. Now several of those obstacles are falling simultaneously This is why 2026 may represent the beginning of the second adoption wave. Barrier #1: injections → pills Novo launched Wegovy tablets in the United States in January 2026. By April, weekly prescriptions had already exceeded 200,000. (Novo Nordisk) By early June, Novo reported more than 3 million prescriptions in slightly more than five months, and importantly said that the majority of new prescriptions were going to people new to GLP-1 therapy. (Novo Nordisk) That last piece matters enormously. If pills merely converted people already using injections, the tablet would mostly cannibalize the existing category. Instead, evidence that many users are new to GLP-1s supports the market-expansion thesis. The product isn’t only redistributing patients. It is helping create patients. Novo subsequently passed 5 million Wegovy-pill prescriptions, while Q2 pill revenue reached roughly DKK 3.22 billion. (Reuters) Lilly has now entered the oral market as well. Its once-daily Foundayo/orforglipron received U.S. approval in April 2026 and can be taken without food or water restrictions. (Lilly Investor Relations) So the industry is moving from: “Would you inject yourself once every week?” toward: “Would you take a pill every morning?” Those questions can produce very different addressable populations. ⸻ 6. High cash prices are beginning to fall Historically, an uninsured patient could face an enormous monthly bill for branded GLP-1 therapy. Now both major companies are experimenting with dramatically cheaper direct-pay entry points. Novo launched the starting dose of Wegovy pill with a $149-per-month self-pay offer. (Novo Nordisk) Lilly launched the lowest dose of Foundayo at $149 per month for self-pay patients, while certain commercially insured patients may pay substantially less. (Lilly Investor Relations) Those figures should not be confused with guaranteed pricing across every dose and every patient. But directionally the change is important. The industry is discovering that: lower price × dramatically greater patient volume may create a larger economic opportunity than: extremely high price × restricted access. That is exactly how a niche pharmaceutical market can begin transitioning toward a mass-market chronic-therapy category. Not financial advice, all personal opinion, long novo.
$LEXX 🔥 MASSIVE BREAKOUT! $LEXX crushed the chart today, closing up +32.35% at $8.10 on over 92K shares traded! The execution of a second independent GLP-1 MTA with commercial-stage biopharma PegBio proves DehydraTECH isn't a one-partner pony—it's a global platform. With the micro-float officially ignited, the chart just printed a textbook high-volume engulfing breakout right off the $6.00 floor. 🚀 NEXT CATALYSTS IN SIGHT: Monday: Nasdaq Compliance Notice: Clearing 10 consecutive days >$1.00 following the 1-for-15 split. Institutional capital will start flowing again. Human Study #7 Readout: Top-line 5-week steady-state PK & Wegovy head-to-head data (late Aug/Sept). Animal Study #1 Results: Concurrent GLP-1 readout dropping alongside human data. Shorts are trapped, volume is surging, and the runway is clear! 📈🚀 $LLY $NVO $VKTX $RANI @topstockalerts @MrHamilton @TopGunFP
View on StockTwits ↗$LLY yo yo.....strong in premarket or early am then tanking each day
View on StockTwits ↗Large cap bearish into 230 $LLY $C $MCD $IBM $BAC
View on StockTwits ↗$SPY $QQQ $NFLX $AAPL $LLY https://www.wavegenius.com/p/s-p-nflx-aapl-lly-nasdaq-w3-long-term-targets
View on StockTwits ↗$LLY https://www.wavegenius.com/p/lly-w3-in-progress-to-2100-1
View on StockTwits ↗Recent $TICKER stream from stocktwits.com — refreshed every 5 minutes. Sentiment tags are self-reported by posters. Not investment advice.