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Parabilis Medicines, Inc. Common Stock

PBLSFDA catalysts, PDUFA dates & pipeline intelligence
$26.85
▼ -2.1 · -7.25%

Financials

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Volume
1.19 M
Value Traded
14.19 M
Short % Float
10.66%
-6.84%Week
-25.75%1 Month
-10.23%3 Month
-15.03%6 Month

Cash Data

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Key Stats

Market Cap
3.32 B
EPS (TTM)
-
P/E Ratio
-
Ent. Value
2.20 B
Total Shares
123.53 M
Float Shares
77.48 M
Insiders
37.28%
Institutions
50.95%

Upcoming Catalysts

FDA decisions, readouts and PDUFA dates · scored by probability of approval

Catalyst Drug / Treatment Stage Prob. of Approval Description Drug Type Therapeutic Area Source
Phase 1/2 data readout
zolucatetide
desmoid tumor
Phase 1/2Small MoleculesOncology
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Every FDA decision, readout and PDUFA date, with drug type, therapeutic area and a PoA score you can trade on.
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PoA blends historical approval base rates, trial design score and FDA review track record.

PBLS Catalyst Timeline

Dated clinical, regulatory and corporate events for Parabilis Medicines, Inc. Common Stock

Catalyst Timeline

Dated clinical, regulatory & corporate events for Parabilis Medicines, Inc. Common Stock

17Total events
7Upcoming
2Tier-1 (high impact)
2026 to 2027Coverage

Upcoming catalysts 2

T1Full Results
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zolucatetide
T3Type B Meeting
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zolucatetide

Event history 8

●Quarterly UpdateCorporate
Reported second quarter 2026 financial results
▲IpoCorporate
Completed upsized initial public offering raising $770.5 million
▲Partnership / LicenseCorporate
Announced strategic research collaboration with Regeneron to develop Antibody-Helicon Conjugates
▲IpoCorporate
Completed upsized initial public offering raising $770.5 million
●Management ChangeCorporate
Appointed Helen Ho as Chief Business & Strategy Officer and Tom Kotarakos as Chief Financial Officer
▲Equity OfferingCorporate
Completed concurrent private placement with Regeneron for $75M
▲PublicationzolucatetidePresentation
Correspondence published in NEJM demonstrating durable response in recurrent ameloblastoma
ameloblastomasource ↗
▲PublicationzolucatetidePresentation
Correspondence published in NEJM demonstrating durable response in recurrent ameloblastoma
ameloblastomasource ↗
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Past FDA Catalysts and PDUFA Decisions

How PBLS actually traded into and out of each decision

Date Drug Catalyst Stage Reaction Event Move % Best Trade %
-Example Drug Phase 3 data readout Phase 3
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Reaction: 30 trading days around the event · Event Move: close to close on decision day · Best Trade: peak run-up from entry 10 days before the decision

Drug Pipeline Intelligence

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Clinical Trial Results

Readouts, endpoints and source filings for every PBLS program

Drug Name Indication Phase Date Trial Results SummaryTitleSource
Example Drug Example indication for clinical evaluationPhase 32025-12-01The study met its primary endpoint demonstrating statistically significant improvement.Read MorePhase 3 Study Results AnnouncementRead More
Scroll for more · summaries link to the source press release
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Inside Trades

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InsiderSideSharesPriceValueDate
RA CAPITAL MANAGEMENT, L.P.Director, 10% OwnerBuy 47,250 26,529,686 held$29.77 07/22/2026
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Hedge Fund 13F Activity

Fund % of Portfolio Current MV Shares Owned Activity
No hedge fund reported a 13F position in PBLS for Q2 2026.
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Options Data

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Option Chain Statistics

ExpiryCall VolPut VolVol P/CCall OIPut OIOI P/CIV CallIV Call OI-WtdIV Call Vol-WtdIV PutIV Put OI-WtdIV Put Vol-Wtd
2027-02-19
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Real-Time Option Chain

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LastVolOILastVolOI
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Calls vs Puts by Expiry

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Competitive positioning

How PBLS ranks across every disease it competes in

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See how PBLS ranks against every competitor across each disease it develops in: phase, best drug, trials and likelihood of approval.
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PBLS News

-PBLS
Oct 14, 2026
PBLSPhases
▼ -7.2%today

Parabilis Medicines Initiates Dose-Ranging Clinical Study of Zolucatetide in Familial Adenomatous Polyposis

Parabilis Medicines has initiated a dose-ranging clinical study of zolucatetide for familial adenomatous polyposis (FAP) as part of its ongoing Phase 1/2 trial. Zolucatetide, a direct inhibitor of the β-catenin:TCF interaction, has shown promising early results in reducing precancerous polyp burden in patients. The study aims to evaluate zolucatetide's efficacy and define dosing for future registrational development.

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-PBLS
Sep 1, 2026
PBLSConferences/Events

Parabilis Medicines to Participate in the Morgan Stanley 24th Annual Global Healthcare Conference

Parabilis Medicines will participate in the Morgan Stanley 24th Annual Global Healthcare Conference on September 16, 2026. CEO Mathai Mammen will lead a fireside chat, discussing the company's innovative approaches to drug development. Parabilis focuses on creating therapies for serious diseases by targeting previously undruggable proteins. The event will be accessible via a live audio webcast.

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-PBLS
Aug 25, 2026
PBLSGeneral

Parabilis Medicines Appoints Accomplished Drug Development Leader Craig L. Tendler, M.D., to Board of Directors

Parabilis Medicines has appointed Dr. Craig L. Tendler to its Board of Directors. Dr. Tendler brings over 30 years of experience in oncology drug development, having previously led clinical development at Johnson & Johnson. His expertise is expected to significantly contribute to the advancement of Parabilis' lead investigational medicine, zolucatetide, and its broader therapeutic pipeline.

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-PBLS
Aug 13, 2026
PBLSGeneral

Parabilis Medicines Reports Second Quarter 2026 Financial Results and Provides Business Updates

Parabilis Medicines reported its second-quarter financial results, highlighting advancements in zolucatetide for treating Wnt/β-catenin-driven diseases, particularly desmoid tumors. The company announced a strategic collaboration with Regeneron, potentially worth $2.2 billion, and ended the quarter with a robust cash position of $1.1 billion. Despite a net loss of $52.5 million, the company remains optimistic about its clinical and regulatory milestones.

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-PBLS
Jun 11, 2026
PBLSGeneral

Parabilis Medicines Announces Closing of Upsized Initial Public Offering, Including Full Exercise of Underwriters’ Option to Purchase Additional Shares

Parabilis Medicines, Inc. has successfully closed its upsized initial public offering, raising $770.5 million through the sale of 38,525,000 shares at $20.00 each. The offering included a full exercise of the underwriters' option to purchase additional shares. Additionally, Parabilis secured $75 million from a concurrent private placement with Regeneron Pharmaceuticals. The company aims to develop transformative medicines targeting historically undruggable proteins.

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-PBLS
Jun 10, 2026
PBLSGeneral

Parabilis Medicines Announces Pricing of Upsized Initial Public Offering

Parabilis Medicines, Inc. has announced the pricing of its upsized initial public offering, offering 33.5 million shares at $20.00 each. The IPO is expected to raise around $670 million and will close on or about June 11, 2026. Additionally, a concurrent private placement with Regeneron Pharmaceuticals will provide approximately $75 million.

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-PBLS
May 18, 2026
PBLSGeneral

Parabilis Medicines Announces Strategic Collaboration with Regeneron Pharmaceuticals to Advance Novel Antibody-Helicon™ Conjugates Across Multiple Therapeutic Areas

Parabilis Medicines has announced a strategic collaboration with Regeneron Pharmaceuticals to develop novel Antibody-Helicon™ Conjugates targeting difficult-to-drug proteins. The agreement includes a $125 million investment from Regeneron, with potential milestone payments reaching approximately $2.2 billion. This partnership aims to leverage Parabilis's Helicon™ peptide platform alongside Regeneron's antibody expertise.

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-PBLS
May 7, 2026
PBLSGeneral

Parabilis Medicines Appoints Biopharmaceutical Finance Leader Alan M. Sebulsky to Board of Directors

Parabilis Medicines has appointed Alan M. Sebulsky to its Board of Directors. Sebulsky, a seasoned biopharmaceutical finance leader, brings extensive experience in public company investment and financial strategy. His background includes leadership roles in significant healthcare firms, enhancing Parabilis's capacity to advance its innovative peptide platform and cancer therapies.

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-PBLS
Apr 14, 2026
PBLSGeneral

Parabilis Medicines Expands Executive Leadership Team

Parabilis Medicines has announced the expansion of its executive leadership team with the appointment of Helen Ho, Ph.D. as Chief Business and Strategy Officer. This move aims to enhance the company's corporate growth strategy and business development efforts. Additionally, Thomas Kotarakos has been promoted to Chief Financial Officer to support the company's financial strategy.

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-PBLS
Mar 11, 2026
PBLSFDA Updates

Parabilis Medicines’ Zolucatetide, the First and Only Direct Inhibitor of the Elusive β-catenin:TCF Interaction, Receives FDA Orphan Drug Designation for the Treatment of Desmoid Tumors

Parabilis Medicines announced that zolucatetide has received FDA Orphan Drug Designation for treating desmoid tumors. This investigational drug is the first direct inhibitor of the β-catenin:TCF interaction, addressing a previously undruggable target. Early clinical data indicates significant antitumor activity, with plans for further trials underway.

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-PBLS
Mar 5, 2026
PBLSPhases

Parabilis Medicines Reports Early Clinical Evidence that Zolucatetide Reduces Polyp Burden in a Patient with Familial Adenomatous Polyposis

Parabilis Medicines has reported early clinical evidence from its ongoing Phase 1/2 trial of zolucatetide, showing significant reductions in duodenal polyposis and a decrease in the size of a co-existing desmoid tumor. This data was presented at the InSiGHT Biennial Meeting, highlighting the potential effectiveness of zolucatetide in treating patients with Familial Adenomatous Polyposis.

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About Parabilis Medicines, Inc. Common Stock

Cambridge, MA parabilismed.com
Headquarters30 ACORN PARK DRIVE, CAMBRIDGE, MA, 02140
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