Enanta Pharmaceuticals
Market cap $320M 29.1M shares (10-Q, Aug 7, 2026) × $11.00 close Nov 6, 2026
Most recent annual filing: 2025-11-15
- EPS-3903 IND filing2H 2026EPS-3903 IND filing, 2H 2026, notable
- MRGPRX2 Inhibitor corporate update2H 2026MRGPRX2 Inhibitor corporate update, 2H 2026, routine
- MRGPRX2 program corporate update2H 2026MRGPRX2 program corporate update, 2H 2026, routine
- EDP-978 Ph1 topline4Q 2026EDP-978 Ph1 topline, 4Q 2026, material
- RESOLVE Ph2b start4Q 2026RESOLVE Ph2b start, 4Q 2026, notable
- Zelicapavir Ph3 start4Q 2026Zelicapavir Ph3 start, 4Q 2026, routine
- Fiscal Q4 earnings financingNov 16, 2026Fiscal Q4 earnings financing, Nov 16, 2026, routine
- ENTA corporate financingNov 16, 2026ENTA corporate financing, Nov 16, 2026, routine
- RESOLVE / LOTUS Ph2b readout2027RESOLVE / LOTUS Ph2b readout, 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 (7 active programs)
EDP-323
EDP-235
EDP-514
EDP-978
EPS-3903
MAVYRET
MAVIRET · glecaprevir · pibrentasvirCapital (as filed)
- Cash
- $33.4M cash and cash equivalents · Jun 30, 2026 (10-Q)
- Short-term investments
- $156M Jun 30, 2026
- Long-term investments
- $22.0M Jun 30, 2026
- Operating cash flow
- −$10.0M quarter Mar 31, 2026 → Jun 30, 2026, year-to-date difference (10-Q)
- As stated in coverage
- $212M cash, runway fiscal 2029 per the update of Oct 29, 2026 — the company's own words as read there, not the filed figure
Offering documents (1)
- 2026-07-02 424B5 · At-the-market program up to $75.0M
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 (9)
- 2026-10-30 UPDATE: Enanta (ENTA) - The Last Lottery Ticket Comes Up Blank 🔒 Paid
- 2026-10-29 UPDATE: Enanta (ENTA) - The Founder-Era CEO Steps Aside 🔒 Paid
- 2026-08-11 UPDATE: Enanta (ENTA) - The ATM They Didn’t Use 🔒 Paid
- 2026-07-02 UPDATE: Enanta (ENTA) - The Shelf Wasn’t Just Housekeeping 🔒 Paid
- 2026-06-23 UPDATE: Enanta (ENTA) - The Federal Circuit Tore Up One of the Lottery Tickets 🔒 Paid
- 2026-06-18 UPDATE: Enanta (ENTA) - The FDA Said Yes. The Market Said No. 🔒 Paid
- 2026-05-12 UPDATE: Enanta (ENTA) - Q2 FY26 Sets the Clock on Zelicapavir 🔒 Paid
- 2026-02-14 UPDATE: Enanta (ENTA) - Q1 2026 Financial Update 🔒 Paid
- 2026-02-10 Enanta Pharmaceuticals (ENTA): Scientific Deep Dive for Lead and Pipeline Products
Articles open on Substack. Some are subscriber-only; those marked ★ Distilled Pro are for Distilled Pro members.
Verdict history (9 calls)
Every verdict Biotech Distilled has published on Enanta Pharmaceuticals, oldest first — the full history, never a selection. How calls are scored: the track record.
- 2026-02-10 Watch Enanta Pharmaceuticals (ENTA): Scientific Deep Dive for Lead and Pipeline Products The RSV Phase 3 design FDA meeting is a binary event; wait for the outcome before taking a position, with the immunology pipeline as a free option protected by cash and royalties.
- 2026-02-14 Speculative buy speculative UPDATE: Enanta (ENTA) - Q1 2026 Financial Update Management's explicit RSV business development language de-risks the binary regulatory bet by signaling a potential partner could fund Phase 3, transforming RSV into optionality on top of cash and royalties.
- 2026-05-12 Speculative buy speculative UPDATE: Enanta (ENTA) - Q2 FY26 Sets the Clock on Zelicapavir The thesis tracks with cash intact and the RSV FDA update now a weeks-away event; the asymmetry between a partner/FDA-acceptance upside and the cash-floor downside remains compelling.
- 2026-06-18 Buy core UPDATE: Enanta (ENTA) - The FDA Said Yes. The Market Said No. FDA acceptance of the HR3 subgroup Phase 3 design retires the single biggest abstract risk; the 18% drawdown on good news creates the entry the original BUY case described, with clinical risk now shifting to the more familiar 'will the effect replicate' question.
- 2026-06-23 Buy core UPDATE: Enanta (ENTA) - The Federal Circuit Tore Up One of the Lottery Tickets The U.S. patent loss was already priced in as a lottery ticket; the EU acute-HCV label expansion provides a small royalty tailwind; the FDA de-risking thesis is intact and the $12.66 entry appears validated by the tape.
- 2026-07-02 Watch UPDATE: Enanta (ENTA) - The Shelf Wasn't Just Housekeeping The $75M ATM activation signals no near-term partnership is landing and that self-funding the Phase 2b/3 requires optional dilution, dampening the asymmetry that made the stock compelling below $13.
- 2026-08-11 Speculative buy speculative UPDATE: Enanta (ENTA) - The ATM They Didn't Use Zero ATM issuance through June 30 and unchanged fiscal 2029 runway guidance confirm the shelf is defensive optionality rather than active financing, satisfying the key condition for reversing the July downgrade, though a 21% royalty decline and five quarters of BD silence keep conviction at speculative.
- 2026-10-29 Speculative buy speculative UPDATE: Enanta (ENTA) - The Founder-Era CEO Steps Aside The planned CEO retirement is an orderly transition that doesn't change the science or cash runway, but adds execution risk during an expensive trial launch; the thesis awaits the November ATM draw disclosure and EDP-978 Phase 1 data.
- 2026-10-30 Speculative buy speculative UPDATE: Enanta (ENTA) - The Last Lottery Ticket Comes Up Blank The UPC ruling invalidating the European Paxlovid patent removes the last litigation upside path but doesn't change the core clinical thesis; the stock now rests purely on cash, a shrinking royalty, and two clinical shots in 2027.
- Long call · opened Feb 17, 2026 at $13.86 · closed Jul 6, 2026 (downgraded to WATCH from long) at $14.51 · +4.7% vs XBI +29.2%
- Long call · opened Aug 12, 2026 at $13.50 · -18.5% vs XBI -3.7% (Nov 6, 2026)
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 (6 quotes from 1 filing)
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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“We expect to report topline data from this trial in the fourth quarter of 2026.”
matched to EDP-978 · topline data · read as fourth quarter of 2026 -
“We are currently performing scale-up and Investigational New Drug application, or IND, enabling activities and are on track to file an IND in the second half of 2026.”
matched to EPS-3903 · regulatory submission · read as second half of 2026 -
“We are continuing to evaluate multiple compounds in preclinical studies and expect to select a development candidate in the second half of 2026.”
matched to MRGPRX2 Inhibitor · other · read as second half of 2026 -
“A hearing on the infringement action and counterclaim for revocation has been scheduled for September 29, 2026 and, under the UPC procedures, a decision is expected to be rendered within weeks thereafter.”
matched to Pfizer UPC (Europe) · UPC hearing and decision · read as September 29, 2026 -
“We expect to initiate this study named RESOLVE in the fourth quarter of 2026, with data from the Phase 2b portion of the RESOLVE study targeted for 2027.”
matched to RESOLVE · Adult Phase 2b/3 initiation · read as fourth quarter of 2026 -
“We initiated this pediatric study named LOTUS and dosed our first participant in the third quarter of 2026, with topline data expected in 2027.”
matched to Zelicapavir · regulatory decision · read as third quarter of 2026
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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 (22)
SEC filings from EDGAR and press releases captured from the company's investor-relations site, newest first. Releases captured from May 4, 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 4, 2026ReleaseEnanta Pharmaceuticals to Participate in Upcoming Investor Conferences
- Oct 29, 20268-KCurrent report: other events→ BD updateThe UPC ruled Enanta's European Paxlovid patent (EP 4 051 265) invalid after the September 29 hearing — both Pfizer litigation lottery tickets are now torn up, and the last non-RSV, non-immunology optionality in the thesis is gone.
- Oct 28, 2026ReleaseEnanta Pharmaceuticals Announces Planned Retirement of Longstanding Chief Executive Officer Jay R. Luly, Ph.D. After 23 Years of Company Leadership→ BD updateSummary on the 8-K
- Oct 28, 20268-KCurrent report: officer / director change, Reg FD disclosure · EX-99.1→ BD updateJay Luly — the founder-era CEO who built Enanta's chemistry platform over 23 years — is retiring by February 1, 2027, right as RESOLVE heads into enrollment and EDP-978 Phase 1 nears readout; the stock dropped ~5% on the news and the successor search introduces real strategic uncertainty at the worst possible moment.
- Oct 26, 2026ReleaseEnanta Pharmaceuticals Announces First Patient Dosed in the RESOLVE Phase 2b/3 Study of Zelicapavir, a Potential First-in-Disease Treatment for Respiratory Syncytial Virus (RSV)RESOLVE just dosed its first patient — the 4Q 2026 trial initiation milestone I've been tracking since June has landed on schedule, moving the 2027 replication binary from calendar commitment to active enrollment.
- Oct 13, 2026ReleaseEnanta Pharmaceuticals to Present Data for Zelicapavir, an Oral, Once-Daily, N-Protein Inhibitor, in Development for the Treatment of Respiratory Syncytial Virus, at IDWeek™ 2026BD extracted 1 program update from this document → ENTA pipeline
- Sep 1, 2026ReleaseEnanta Pharmaceuticals to Participate in September Investor Conferences
- Aug 12, 202610-QQuarterly report
- Aug 10, 2026ReleaseEnanta Pharmaceuticals Reports Financial Results for its Fiscal Third Quarter Ended June 30, 2026
- Aug 10, 20268-KCurrent report: results of operations · EX-99.1
- Jul 2, 20268-KCurrent report: material agreement
- Jul 2, 2026424B5Prospectus supplement (offering)
- Jun 23, 2026ReleaseEnanta Pharmaceuticals’ Partner AbbVie Receives European Commission Approval of MAVIRET® (Glecaprevir/Pibrentasvir) for People with Acute Hepatitis C Virus
- Jun 23, 20268-KCurrent report: other events
- Jun 18, 2026ReleaseEnanta Pharmaceuticals Announces Advancement of its Zelicapavir Clinical Development Program for the Treatment of Respiratory Syncytial Virus (RSV)
- Jun 18, 20268-KCurrent report: Reg FD disclosure · EX-99.1BD extracted 1 program update from this document → ENTA pipeline
- May 28, 2026ReleaseEnanta Pharmaceuticals to Present at the Jefferies Global Healthcare Conference
- May 13, 202610-QQuarterly report
- May 11, 20268-KCurrent report: results of operations · EX-99.1
- May 4, 2026ReleaseEnanta Pharmaceuticals to Present Data for its Respiratory Syncytial Virus and STAT6 Inhibitor Programs at the American Thoracic Society International Conference 2026
- Mar 26, 20268-KCurrent report: other events
- Mar 12, 20268-KCurrent report: officer / director change, shareholder vote
5 more filings (13G holder notices, S-8, proxy material, SEC correspondence …)
- Oct 27, 2026SCHEDULE 13GPassive >5% holder (13G)
- Aug 14, 2026SCHEDULE 13G/A13G amendment
- Aug 14, 2026SCHEDULE 13G/A13G amendment
- May 13, 2026S-8Employee plan registration
- Mar 26, 2026SCHEDULE 13G/A13G amendment