Vanda Pharmaceuticals
Market cap $231M 60.5M shares (10-Q, Oct 22, 2026) × $3.82 close Nov 6, 2026
Most recent annual filing: 2026-02-13
- Jet Lag patent litigation rulingDec 2026Jet Lag patent litigation ruling, Dec 2026, routine
- Imsidolimab FDA approvalDec 12, 2026Imsidolimab FDA approval, Dec 12, 2026, material
- Bysanti™ milsaperidone readout1H 2027Bysanti™ milsaperidone readout, 1H 2027, notable
Bar width shows how precise the guidance is — a pin is a stated date, a wide band a six-month window. Deeper blue means more of the thesis rides on the event; it is not a view on the stock.
Pipeline (27 active programs)
HETLIOZ
tasimelteonPONVORY
ponesimodNEREUS
tradipitantBysanti
milsaperidoneQuimilza
imsidolimabVTR-297
VSJ-110
VPO-227
VQW-765
VCA-894A
VGT-1849A
VGA-157A
Capital (as filed)
- Cash
- $61.9M cash and cash equivalents · Sep 30, 2026 (10-Q)
- Operating cash flow
- −$28.4M quarter Jun 30, 2026 → Sep 30, 2026, year-to-date difference (10-Q)
- As stated in coverage
- $141M cash, runway second half of 2027 per the update of Oct 28, 2026 — the company's own words as read there, not the filed figure
Cash, investments and operating cash flow are the company's own XBRL facts as filed with the SEC, each shown with its period end and tag. As-stated figures come from the company's own words as read in Biotech Distilled coverage, dated, and routinely count securities and planned financing that a balance sheet does not. Offering rows are the SEC cover pages as filed. Not investment advice. Figures as of Nov 7, 2026.
Biotech Distilled coverage (13)
- 2026-10-29 UPDATE: Vanda Pharmaceuticals (VNDA) - The Cash Figure I Asked For 🔒 Paid
- 2026-10-28 UPDATE: Vanda Pharmaceuticals (VNDA) - The Sidecar Survives, at Half the Horsepower 🔒 Paid
- 2026-10-15 UPDATE: Vanda Pharmaceuticals (VNDA) - The Social Anxiety Lottery Ticket Comes Up Blank 🔒 Paid
- 2026-08-06 UPDATE: Vanda Pharmaceuticals (VNDA) - The HETLIOZ® Cliff Arrives 🔒 Paid
- 2026-05-06 UPDATE: Vanda Pharmaceuticals (VNDA) — The Burn Rate Confession and the DTC Hail Mary
- 2026-03-21 UPDATE: Vanda’s $30 Million "Ethics" Play — Turning the Tradipitant Roadblock into a PR War 🔒 Paid
- 2026-03-07 UPDATE: Vanda’s (VNDA) Litigation Moat Makes History — The 40-Year FDA Streak is Broken 🔒 Paid
- 2026-02-28 UPDATE: Vanda Pharmaceuticals (VNDA) - The Narrative Machine Speeds Up 🔒 Paid
- 2026-02-21 UPDATE: Vanda Pharmaceuticals (VNDA) - The PDUFA Pop Arrives — Now Watch for the Anvil 🔒 Paid
- 2026-02-14 UPDATE: Vanda Pharmaceuticals (VNDA) - The Dilution Gap Confirmed — Vanda Drops a $200M Shelf 🔒 Paid
- 2026-02-11 UPDATE: Vanda Pharmaceuticals (VNDA) Expensive Victory Lap — NEREUS™ Approved, Cash Burn Accelerates 🔒 Paid
- 2026-01-10 UPDATE: Vanda vs. The FDA (Round Infinity) — The Jet Lag Denial 🔒 Paid
- 2025-12-31 FDA APPROVED Dec. 30, 2025 :: Vanda Pharmaceuticals (VNDA): Scientific Due Diligence for Tradipitant and Pipeline Products 🔒 Paid
Articles open on Substack. Some are subscriber-only; those marked ★ Distilled Pro are for Distilled Pro members.
Verdict history (13 calls)
Every verdict Biotech Distilled has published on Vanda Pharmaceuticals, oldest first — the full history, never a selection. How calls are scored: the track record.
- 2025-12-31 Watch FDA APPROVED Dec. 30, 2025 :: Vanda Pharmaceuticals (VNDA): Scientific Due Diligence for Tradipitant and Pipeline Products Vanda is a high-risk, event-driven play with valid science but significant commercial hurdles; wait for Q4 GLP-1 data confirmation and patent trial clarity before entering.
- 2026-01-10 Watch UPDATE: Vanda vs. The FDA (Round Infinity) — The Jet Lag Denial FDA rejection of HETLIOZ Jet Lag sNDA removes a key upside catalyst, but the GLP-1 sidecar thesis remains intact; stance unchanged.
- 2026-02-11 Hold UPDATE: Vanda Pharmaceuticals (VNDA) Expensive Victory Lap — NEREUS™ Approved, Cash Burn Accelerates Fanapt's bipolar launch is working but aggressive spending and accelerating cash burn raise the price of admission; next binary is the Feb 21 Bysanti PDUFA.
- 2026-02-14 Avoid UPDATE: Vanda Pharmaceuticals (VNDA) - The Dilution Gap Confirmed — Vanda Drops a $200M Shelf The $200M shelf registration confirms the dilution risk; any PDUFA pop is likely to be used by management to raise capital at shareholders' expense.
- 2026-02-21 Hold UPDATE: Vanda Pharmaceuticals (VNDA) - The PDUFA Pop Arrives — Now Watch for the Anvil Bysanti approval triggered a 56% after-hours pop but with a $200M shelf loaded and management already compensated, holders should consider selling into strength.
- 2026-02-28 Avoid UPDATE: Vanda Pharmaceuticals (VNDA) - The Narrative Machine Speeds Up Three simultaneous launches will require enormous SG&A spend that the $263M cash pile cannot sustain without tapping the $200M shelf; financial gravity is inescapable.
- 2026-03-07 Avoid UPDATE: Vanda's (VNDA) Litigation Moat Makes History — The 40-Year FDA Streak is Broken Historic FDA evidentiary hearing win is a cash incinerator with no near-term revenue; shareholders bear the financial risk of litigation while management benefits.
- 2026-03-21 Avoid UPDATE: Vanda's $30 Million "Ethics" Play — Turning the Tradipitant Roadblock into a PR War The 20% weekly stock drop signals narrative premium evaporating; Vanda's animal-rights PR is regulatory jujitsu to avoid expensive FDA requirements, not genuine advocacy.
- 2026-05-06 Avoid UPDATE: Vanda Pharmaceuticals (VNDA) — The Burn Rate Confession and the DTC Hail Mary Q1 burn of $61.5M annualizes to ~$200M against a $202M cash pile; the S-3 is now effective and a raise is a question of when, not if, before the Thetis GLP-1 readout.
- 2026-08-06 Avoid UPDATE: Vanda Pharmaceuticals (VNDA) - The HETLIOZ® Cliff Arrives HETLIOZ fell 66% to $5.6M as generics take hold, NEREUS launched to only $1M, and the 2027 runway is a management promise not arithmetic; the GLP-1 Thetis readout remains the only thesis-defining catalyst.
- 2026-10-15 Avoid UPDATE: Vanda Pharmaceuticals (VNDA) - The Social Anxiety Lottery Ticket Comes Up Blank VQW-765 missed its Phase III primary endpoint by a statistically null margin, removing one lottery ticket; the GLP-1 Thetis readout this quarter remains the only valuation-justifying catalyst.
- 2026-10-28 Watch UPDATE: Vanda Pharmaceuticals (VNDA) - The Sidecar Survives, at Half the Horsepower Thetis Phase III hit its primary endpoint retiring clinical risk on the GLP-1 mechanism, but the absolute benefit halved versus Phase II and the real-world titration question remains open; upgrading from AVOID but not to Buy pending cash figure, shelf use, and FDA titration guidance.
- 2026-10-29 Watch UPDATE: Vanda Pharmaceuticals (VNDA) - The Cash Figure I Asked For Q3 burn slowed to $29.5M and spending fell 18%, but revenue guidance top end was cut, NEREUS is at $2.6M YTD, and the MDD readout slipped; one of three entry triggers resolved neutrally while shelf use and FDA titration view remain open.
- Avoid call · opened Feb 17, 2026 at $6.20 · closed Oct 28, 2026 (downgraded to WATCH from avoid) at $4.00 · -35.5% vs XBI +26.4%
Every verdict Biotech Distilled has published on this company, in order, with the post it came from — the full history, never a selection. Position figures are the same ones shown on /track-record, computed by the same method. Editorial opinion, not investment advice.
Timing, in the company's words (7 quotes from 6 filings)
Sentences quoted verbatim from the company's SEC filings, newest filing first. Each sits under the filing it appeared in; the "matched to" tag names the calendar row it was read for.
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“The Biologics License Application (BLA) for Quimilza™ in Generalized Pustular Psoriasis (GPP) is under review by the FDA with a Prescription Drug User Fee Act (PDUFA) target action date of December 12, 2026.”
matched to Imsidolimab · regulatory decision · read as December 12, 2026
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“Quimilza TM BLA for GPP under review by the FDA; PDUFA target action date of December 12, 2026 WASHINGTON – October 28, 2026 – Vanda Pharmaceuticals Inc. (Vanda) (Nasdaq: VNDA) today announced financial and operational results for the third quarter ended September 30, 2026.”
matched to Imsidolimab · regulatory decision · read as December 12, 2026
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“The Company’s lawsuit remains pending, and a trial is scheduled to begin on October 26, 2026.”
matched to HETLIOZ® · other · read as October 26, 2026 -
“The Biologics License Application (BLA) for Quimilza TM in GPP is under review by the FDA with a Prescription Drug User Fee Act (PDUFA) target action date of December 12, 2026.”
matched to Imsidolimab · regulatory decision · read as December 12, 2026
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“With BYSANTI approved and on track for launch in the second half of 2026, a December 2026 PDUFA date for Quimilza and multiple late-stage clinical trial results expected before year-end, we believe Vanda is well positioned for meaningful commercial expansion and pipeline value creation,” said Mihael H. Polymeropoulos, M.D., Vanda’s President, CEO and Chairman of the Board.”
matched to Bysanti™ (milsaperidone) · readout other · read as December 2026
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“BYSANTI TM is protected by data exclusivity through February 20, 2031 and multiple patents, the latest of which expires on May 31, 2044.”
matched to Bysanti™ (milsaperidone) · readout other · read as May 31, 2044
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“BYSANTI TM is protected by data exclusivity through February 20, 2031 and multiple patents, the latest of which expires on May 31, 2044.”
matched to Bysanti™ (milsaperidone) · readout other · read as May 31, 2044
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Timing sentences quoted from the company's own SEC filings, each under the filing it appeared in. The 'matched to' tag is the calendar row the sentence was read for; the filing is the source. Not investment advice.
Filings & releases (28)
SEC filings from EDGAR and press releases captured from the company's investor-relations site, newest first. Releases captured from Jul 7, 2026; filings from March 2026. Summaries come from the BD update that read the document; "BD extracted" counts point at the pipeline table above. All companies →
- Nov 3, 2026ReleaseVanda Pharmaceuticals Announces Participation at November 2026 Investor Conferences
- Oct 29, 202610-QQuarterly report
- Oct 28, 2026ReleaseVanda Pharmaceuticals Reports Third Quarter 2026 Financial Results→ BD updateSummary on the 8-K
- Oct 28, 20268-KCurrent report: results of operations · EX-99.1→ BD updateQ3 2026 earnings landed after the close: revenues surged 24% to $69.8M, operating expenses fell 18% from Q2, and management raised full-year guidance to >$240M — but cash dropped to $140.5M and the $200M dilution shelf is still loaded heading into a gauntlet of Q4 catalysts.BD extracted 1 program update from this document → VNDA pipeline
- Oct 27, 2026ReleaseVanda Pharmaceuticals Announces Positive Results from Study 3601 of NEREUS™ (tradipitant) for Prevention of GLP-1-Induced Vomiting→ BD updateThe GLP-1 sidecar lottery ticket just printed a winning number: Study 3601 hit its primary endpoint (43.0% vs. 58.5% vomiting, p=0.006) and delivered an 81% relative reduction in extreme vomiting (p=0.0003) — the strongest signal in Vanda's pipeline history, and the one catalyst the entire bull case was waiting for.
- Oct 21, 2026ReleaseVanda Pharmaceuticals to Announce Third Quarter 2026 Financial Results on October 28, 2026
- Oct 14, 2026ReleaseVanda Pharmaceuticals Provides Update on VQW-765 Clinical Development Program→ BD updateVQW-765 just washed out in Phase III (p=0.89) — the social anxiety asset is on hold — while a previously uncovered HETLIOZ® win in delayed sleep-wake phase disorder quietly adds a new sNDA shot to an eroding franchise.BD extracted 1 program update from this document → VNDA pipeline
- Oct 2, 2026ReleaseVanda Pharmaceuticals Announces Presentation at 2026 EADV Annual Meeting
- Sep 29, 2026ReleaseVanda Pharmaceuticals Announces Positive Phase III Results for HETLIOZ®(tasimelteon) in Delayed Sleep-Wake Phase Disordervia aggregator
- Sep 2, 2026ReleaseVanda Pharmaceuticals Announces Participation at September 2026 Investor Conferences
- Aug 24, 2026ReleaseVanda Pharmaceuticals Granted Orphan Designation for Imsidolimab for the Treatment of Generalized Pustular Psoriasis by the European Commission
- Aug 22, 2026ReleaseNEREUS™ Sponsored No. 47 IndyCar Ready for Historic Freedom 250 Grand Prix in Washington, D.C.
- Aug 6, 202610-QQuarterly report
- Aug 5, 2026ReleaseVanda Pharmaceuticals Reports Second Quarter 2026 Financial Results
- Aug 5, 20268-KCurrent report: results of operations · EX-99.1
- Jul 29, 2026ReleaseVanda Pharmaceuticals to Announce Second Quarter 2026 Financial Results on August 5, 2026
- Jul 16, 2026ReleaseVanda Pharmaceuticals Announces EMA Positive Opinion for Orphan Drug Designation of Imsidolimab for Generalized Pustular Psoriasis - A Milestone Recognition of GPP as a Distinct Rare Disease in EuropeBD extracted 1 program update from this document → VNDA pipeline
- Jul 15, 2026ReleaseNEREUS™ Powers Forward: Sponsors No. 47 IndyCar Entry, Celebrating 47 Years Since Last New U.S. Motion Sickness Treatmentvia aggregator
- Jul 10, 2026ReleaseVanda Pharmaceuticals Announces Participation in the B. Riley Securities 2026 Mind, Muscle & Vision Summit
- Jul 7, 2026ReleaseVanda Pharmaceuticals Announces FDA Rare Pediatric Disease Designation for Investigational Therapy for Charcot-Marie-Tooth Disease Type 2S
- Jun 5, 20268-KCurrent report: shareholder vote
- May 7, 202610-QQuarterly report
- May 6, 20268-KCurrent report: results of operations · EX-99.1
- Apr 23, 2026DEFA14AProxy soliciting material
- Apr 23, 2026DEF 14AProxy statement
- Apr 22, 20268-KCurrent report: officer / director change · EX-99.1
- Apr 2, 20268-KCurrent report: officer / director change
- Mar 10, 20268-KCurrent report: Reg FD disclosure
11 more filings (13G holder notices, S-8, proxy material, SEC correspondence …)
- Oct 27, 2026SCHEDULE 13GPassive >5% holder (13G)→ BD updateSummary on the release
- Oct 9, 2026SCHEDULE 13G/A13G amendment
- Aug 19, 2026SCHEDULE 13GPassive >5% holder (13G)
- Aug 13, 2026SCHEDULE 13GPassive >5% holder (13G)
- Jun 5, 2026S-8Employee plan registration
- May 12, 2026SCHEDULE 13GPassive >5% holder (13G)
- May 5, 2026EFFECTRegistration effective
- Apr 29, 2026SCHEDULE 13G/A13G amendment
- Apr 24, 2026CORRESPCORRESP
- Apr 23, 2026ARSAnnual report to shareholders
- Mar 27, 2026SCHEDULE 13G/A13G amendment