Amylyx Pharmaceuticals, Inc. (AMLX) Stock Price & How to Invest

Last updated October 2026

Short answer

AMLX is Amylyx Pharmaceuticals, a clinical-stage biotech whose value rests largely on avexitide, a candidate for post-bariatric hypoglycemia that met its primary endpoint in the Phase 3 LUCIDITY trial in 2026, cutting severe hypoglycemic events by 55%. The company plans to file for FDA approval before the end of 2026. It trades on the Nasdaq like any other listed equity, closing at $26.69 on October 16, 2026, up about 134% year to date, and the position now behaves like a regulatory-and-launch story rather than a binary readout trade.

AMLX stock price

As of 2026-11-05, Amylyx Pharmaceuticals, Inc. (AMLX) last closed at $27.62, up 121.7% over the past year. Over the past 52 weeks it has traded between $11.38 and $39.66.

AMLX last close
$27.62
1 day
-6.05%
1 month
-1.50%
1 year
+121.67%
52-week range
$11.38 to $39.66
Last close
2026-11-05

Prices are daily closing prices from Yahoo Finance and may be delayed. For the live quote, check your broker or Amylyx Pharmaceuticals, Inc.'s investor relations page. Walnut is informational, not investment advice.

What does Amylyx Pharmaceuticals, Inc. (AMLX) do?

Amylyx Pharmaceuticals develops treatments for neurodegenerative and endocrine conditions with few or no approved options. Its lead program is avexitide, a GLP-1 antagonist being tested in adults with post-bariatric hypoglycemia (PBH), a condition where people who have had Roux-en-Y gastric bypass surgery experience severe blood-sugar crashes. The registrational Phase 3 LUCIDITY trial enrolled 78 participants across a 16-week blinded period and met its pre-specified primary endpoint: a 55% reduction in Level 2 and Level 3 hypoglycemic events (p=0.000003). It also met secondary endpoints on Level 2 events, Level 3 events, and continuous glucose-monitoring outcomes, and avexitide was generally safe and well tolerated, consistent with earlier trials. All eligible patients moved into the open-label extension. Amylyx plans to present the topline data at ObesityWeek 2026 and to submit a New Drug Application before year-end 2026, with management discussing a possible 2027 launch. Behind it sit AMX0035 in Wolfram syndrome (a focused registrational Phase 3 was guided for the second half of 2026 after extended Phase 2 HELIOS data showed trends in pancreatic function and vision stabilization), AMX0114 in ALS (Phase 1 LUMINA data reported as safety-supportive), and AMX0318 in IND-enabling studies.

The investment picture is still concentrated, but the shape of the risk has changed. Amylyx has no meaningful product revenue today: its first approved drug, Relyvrio for ALS, was pulled from the market in 2024 after the confirmatory PHOENIX Phase 3 trial missed, which reset the company from commercial-stage back to clinical-stage and left a lasting credibility question that a clean LUCIDITY result goes some way toward answering. What it does have is a funded balance sheet, roughly $250.8 million in cash, cash equivalents and short-term investments as of June 30, 2026, with runway guided into 2028, which covers the filing, the review and a 2027 launch without a forced financing. The market has repriced the stock around that result: shares closed at $26.69 on October 16, 2026, up about 133.7% year to date and 75.9% over one year, for a market capitalization near $3.35 billion, though they have pulled back about 18% over the past month from a 52-week high of $41.14.

What's driving Amylyx Pharmaceuticals, Inc. (AMLX)?

1. From LUCIDITY data to an FDA filing.

The 78-participant registrational trial met its primary endpoint with a 55% reduction in Level 2 and Level 3 hypoglycemic events and hit its key secondary measures. That moves the central question from whether avexitide works to how the FDA reviews it. Amylyx plans to submit the NDA before year-end 2026 and to present the full topline data at ObesityWeek 2026; filing acceptance, review timing and the eventual label are the next value-setting events.

2. A market with no approved therapy.

Post-bariatric hypoglycemia currently has no FDA-approved treatment, so patients are managed with diet modification and off-label drugs. That gives avexitide a defined addressable population, a motivated specialist prescriber base (bariatric surgeons and endocrinologists), and a plausible orphan-style pricing and launch model that does not require a large primary-care sales force. Bariatric surgery volumes and GLP-1-era metabolic care keep the diagnosed pool growing. Analysts on average model about $28 million of revenue in 2027, a first-year launch figure.

3. Balance sheet that funds the launch.

Cash of roughly $250.8 million at mid-2026 against only about $5 million of debt, and runway guided into 2028, means Amylyx does not have to raise capital immediately on whatever terms the market offers. Quarterly net losses ran near $41-43 million in the first half of 2026, with R&D of about $23.8 million and SG&A of about $21.9 million in the second quarter. Commercial preparation will push SG&A higher, so the cash line each quarter, starting with the Q3 report on November 5, 2026, shows how much room is left.

4. A second and third shot on goal.

AMX0035 in Wolfram syndrome is the most advanced backup, with a focused registrational Phase 3 guided for the second half of 2026 following extended Phase 2 HELIOS results. AMX0114, an antisense candidate targeting calpain-2 in ALS, and AMX0318 in IND-enabling work sit further back. None of these carries near-term revenue, but they determine whether the company has a franchise beyond avexitide.

What are the risks to Amylyx Pharmaceuticals, Inc. (AMLX)?

The concentration risk remains the dominant one: avexitide now carries nearly all of the equity value, and a positive 78-patient trial still leaves FDA review risk, label risk, and the possibility of requests for more data. Amylyx has already failed a confirmatory Phase 3 once, with Relyvrio withdrawn from the market in 2024, so execution credibility is still being rebuilt. Launching a drug for a rare condition is costly, and adoption depends on endocrinologists and payers treating the effect size as a clear improvement over cheap off-label options. The company generates no product revenue and lost about $152 million over the trailing twelve months, so any delay pushes it toward a financing that would dilute existing holders. The stock is volatile: it more than tripled from its 52-week low of $10.83 to $41.14 and then fell about 18% in the month to October 16, 2026, and an insider sold about $831,000 of shares in early October. There is also a legacy legal item: a securities class action tied to 2022 to 2023 Relyvrio launch statements was settled for $6.5 million, with preliminary court approval in May 2026 and a final approval hearing scheduled for September 2026.

What is the Amylyx Pharmaceuticals, Inc. (AMLX) forecast?

11 analysts publish price targets on AMLX, averaging $42.64 against a $27.70 price as of November 2026, or +53.9%. The published targets run from $20.00 to $57.00, a wide spread, and the ratings split 11 buy, 1 hold, 0 sell. Over the last six months there have been 10 raises and 0 cuts among the published actions. A price target is what an analyst published on a date, not a prediction, and sell-side ratings skew positive across the whole market.

Read the full AMLX forecast and price target for the target table, the recent rating actions by firm, and how the consensus has shifted.

Is AMLX a buy or a sell?

We give no verdict on Amylyx Pharmaceuticals, Inc.. Both cases are real, which is why the question is contested at all, so here is the strongest version of each.

The case for buying. From LUCIDITY data to an FDA filing. The 78-participant registrational trial met its primary endpoint with a 55% reduction in Level 2 and Level 3 hypoglycemic events and hit its key secondary measures. The most optimistic published target, $57.00, assumes this works close to its best case.

The case against. The concentration risk remains the dominant one: avexitide now carries nearly all of the equity value, and a positive 78-patient trial still leaves FDA review risk, label risk, and the possibility of requests for more data. The most pessimistic target, $20.00, is roughly what AMLX is worth if this bites instead.

Read the full bull and bear case on AMLX, including what would have to change to break either one. Walnut is not an investment adviser.

Has Amylyx Pharmaceuticals, Inc. (AMLX) split its stock?

No. Amylyx Pharmaceuticals, Inc. (AMLX) has not split its stock in the last 10 years. That is a statement about the window we check rather than about the company’s entire history, so an older split is possible. It also matters less than it once did: fractional shares mean a high price per share no longer keeps smaller investors out, which removed most of the practical reason to split.

How is Amylyx Pharmaceuticals, Inc. (AMLX) valued? (approximate, October 2026)

A simple financial snapshot. These are approximations and refresh quarterly; for current figures see Amylyx Pharmaceuticals, Inc.'s investor relations page or your broker.

  • Product revenue: None (Relyvrio withdrawn in 2024; consensus ~$28M for 2027)
  • Cash and equivalents: ~$250.8M (June 30, 2026)
  • Cash runway: Guided into 2028
  • Net loss (TTM): ~$152M (EPS ~-$1.41)
  • Operating cash burn (TTM): ~$127M
  • Price to book: ~12x
  • Market cap: ~$3.35B

Standard valuation multiples do not apply here because there is no revenue and no path to profitability without an approval. After the positive LUCIDITY result, the market capitalization of about $3.35 billion (October 16, 2026) sits on top of about $251 million of cash and a trailing loss near $152 million, so most of the value is the market's view of avexitide's approval odds and launch potential. The 11 analysts covering the stock have an average target near $43, and the Q3 2026 report on November 5 will update the cash line and filing timeline.

Who competes with Amylyx Pharmaceuticals, Inc. (AMLX)?

Metabolic and hypoglycemia-focused biotechs

Companies developing therapies for hyperinsulinemic hypoglycemia and related glucose-regulation disorders, including Zealand Pharma (glucagon and metabolic peptides) and Crinetics Pharmaceuticals (endocrine small molecules). They compete for the same specialist prescribers, the same endocrinology investor attention, and in some cases the same patients, since congenital and post-surgical hypoglycemia programs overlap clinically.

Rare-disease neurology and CNS developers

Amylyx still runs ALS and Wolfram syndrome programs, which puts it alongside Biogen (Qalsody in SOD1 ALS), Ionis Pharmaceuticals (antisense platform), Denali Therapeutics and Wave Life Sciences. These set the benchmark for what neurology trial design, regulatory flexibility and orphan pricing look like, and they compete directly for the small pool of eligible ALS trial participants.

Standard of care and off-label incumbents

The practical competition for avexitide today is not another branded drug but existing management: dietary modification, acarbose, diazoxide, octreotide and, in severe cases, surgical revision. Generic and off-label options are cheap and entrenched, so adoption depends on the 55% event reduction seen in LUCIDITY being large enough that endocrinologists and payers treat avexitide as a clear improvement rather than an expensive alternative.

What stocks are similar to Amylyx Pharmaceuticals, Inc. (AMLX)?

Other names that sit close to AMLX: same theme, named as a direct competitor, or held beside it in the same funds. Each entry says which. Worth a look if you are thinking about diversification within a thesis rather than concentration on one ticker.

How to invest in Amylyx Pharmaceuticals, Inc. (AMLX)

There are three common ways to get AMLX exposure. Buy shares (or fractional shares) directly at any major broker. Hold an ETF that includes it, which spreads the position across many companies. Or build it into a focused thematic portfolio, so AMLX sits alongside other stocks that express the same thesis.

Walnut takes the portfolio route. Describe a thesis where AMLX fits (for example “AI infrastructure” or “dividend-growth large-caps”) and the AI proposes 5 to 6 constituents with target weights. You review the plan and fund it through your own broker when you're ready.

New to this? Start with how to invest in stocks, see how to analyze a stock with AI, or compare the best AI stock analyzers.

The bottom line on Amylyx Pharmaceuticals, Inc. (AMLX)

Amylyx is a funded, single-asset biotech whose biggest risk, the LUCIDITY readout, came back positive; the story now turns on an FDA filing guided for year-end 2026, the review that follows, and whether a small company can launch a drug for a rare condition in 2027.

More on Amylyx Pharmaceuticals, Inc. (AMLX)

Whether AMLX is worth buying today depends more on your time horizon and what you already hold than on any single call. We walk through valuation, what would have to go right, and the risks in is AMLX a buy or a sell?, and where the stock could go from here in the AMLX stock forecast.

For income investors, whether AMLX pays a dividend and how the payout looks is covered in does AMLX pay a dividend? And to weigh AMLX against a peer, read the full side-by-side comparisons: AMLX vs CRNX and AMLX vs CNS.

Wondering how AMLX fits the portfolio you already own? Walnut is an AI investing app that connects your brokerage read-only and answers questions like that about your actual holdings: overlap, concentration, and how each position tracks the S&P 500. Compare the best AI portfolio analyzers or see the best AI investing apps in 2026.

Investing in Amylyx Pharmaceuticals, Inc. with AI

Connect the broker you already use and ask Walnut's AI how AMLX fits what you actually hold: whether you own it already through a fund, what it would do to your concentration, and how it has tracked the S&P 500. Read-only by default, and you approve anything before it reaches your broker.

FAQ

What does Amylyx Pharmaceuticals actually do?

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Amylyx is a clinical-stage biotech developing drugs for conditions with few approved options. Its lead candidate, avexitide, succeeded in Phase 3 for post-bariatric hypoglycemia and is headed for an FDA filing, and it also runs programs in Wolfram syndrome (AMX0035), ALS (AMX0114) and a preclinical asset (AMX0318). It sells no products today.

Does AMLX have any revenue?

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Not meaningfully. Its only approved product, Relyvrio for ALS, was withdrawn from the market in 2024 after the confirmatory PHOENIX Phase 3 trial failed to show benefit. Since then Amylyx has operated as a pre-revenue clinical-stage company funded entirely by its balance sheet. Analysts on average expect about $28 million of revenue in 2027 if avexitide is approved and launched.

What is avexitide and why does it matter so much?

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Avexitide is a GLP-1 receptor antagonist for post-bariatric hypoglycemia, a condition where gastric bypass patients suffer severe blood-sugar crashes. There is no FDA-approved treatment for it. Because avexitide is the only late-stage asset in the portfolio, and now has positive Phase 3 data, its filing, review and launch carry most of the company's value.

What did the LUCIDITY Phase 3 trial show?

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LUCIDITY met its pre-specified primary endpoint, with a 55% reduction in Level 2 and Level 3 hypoglycemic events (p=0.000003), and met secondary endpoints for Level 2 events, Level 3 events and continuous glucose-monitoring outcomes. Avexitide was generally safe and well tolerated, and all eligible patients enrolled in the open-label extension. Amylyx will present the data at ObesityWeek 2026.

When is the next major catalyst?

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The LUCIDITY readout has happened. The next items are the full data presentation at ObesityWeek 2026, the Q3 2026 report on November 5, 2026, and the New Drug Application, which Amylyx expects to submit before year-end 2026. Separately, management guided a focused registrational Phase 3 of AMX0035 in Wolfram syndrome to start in the second half of 2026.

How has AMLX stock performed in 2026?

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AMLX closed at $26.69 on October 16, 2026, up about 133.7% year to date and 75.9% over one year, and about 44% over three months. The run was not smooth: the 52-week range is $10.83 to $41.14, and the shares fell about 17.6% in the month to October 16 after peaking around the LUCIDITY result.

How much cash does Amylyx have and how long does it last?

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About $250.8 million in cash, cash equivalents and short-term investments as of June 30, 2026, with runway guided into 2028. Quarterly net losses were about $41-43 million in the first half of 2026. That funding is meant to cover the NDA filing, the FDA review and a potential 2027 commercial launch without an immediate forced financing.

Is the Relyvrio failure still relevant?

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Yes, in two ways. It removed the company's only revenue source and forced a restructuring back to clinical stage, and it left investors treating management's guidance with more skepticism than they would for a company without that history; the positive LUCIDITY result helps on that front. A related securities class action was settled for $6.5 million, with preliminary approval granted in May 2026.

How do people invest in AMLX?

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AMLX trades on the Nasdaq and can be bought through any standard U.S. brokerage account, including fractional-share brokers. Because the price is driven by trial and regulatory events rather than earnings, position sizing tends to matter more here than entry timing. Walnut is not an investment adviser.

What would make the thesis break?

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With LUCIDITY positive, the main breakage points are now an FDA refusal to file or a review setback, a restrictive label, a slower rare-disease launch than modeled, or a dilutive financing if timelines slip. Without avexitide, only earlier-stage assets would remain against a quarterly burn of roughly $40 million.

Walnut is informational, not investment advice. Financial figures on this page are approximations; always verify current numbers with Amylyx Pharmaceuticals, Inc.'s investor relations page or your broker before making investment decisions.