Xeris Biopharma Holdings, Inc.

Xeris Biopharma Holdings, Inc. (XERS) Market Cap

Xeris Biopharma Holdings, Inc. has a market capitalization of $1.39B.

Price: $8.08

-0.34 (-4.04%)

Market Cap: 1.39B

NASDAQ · time unavailable

CEO: John Shannon

Sector: Healthcare

Industry: Biotechnology

IPO Date: 2018-06-21

Website: https://www.xerispharma.com

Xeris Biopharma Holdings, Inc. (XERS) - Company Information

Market Cap: 1.39B|Sector: Healthcare

Company Profile

Xeris Biopharma Holdings, Inc. operates as a biopharmaceutical company, focusing on the development and commercialization of therapeutic solutions for individuals across the fields of endocrinology, neurology, and gastroenterology. Its current portfolio includes: Gvoke: A ready-to-administer liquid glucagon designed to treat severe hypoglycemia. Keveyis: A therapy addressing hyperkalemic, hypokalemic, and related forms of primary periodic paralysis. Recorlev: A cortisol synthesis inhibitor approved for managing endogenous hypercortisolemia in adult patients with Cushing's syndrome. Beyond its marketed products, the company maintains an active development pipeline. This pipeline seeks to broaden the applications and indications for existing treatments and introduce novel pharmaceuticals leveraging its proprietary XeriSol and XeriJect formulation technology platforms. Founded in 2005, Xeris Biopharma is headquartered in Chicago, Illinois.

Analyst Sentiment

81%
Strong Buy

From 7 Active Polls

1Y Forecast: $8.82

▲ +9.2% Potential Upside

Consensus Target Metrics

Low Bound

$4

Median

$7

High Bound

$18

Average

$9

Price & Moving Averages

Loading chart...

🎯 Wall Street Analyst Intelligence Report

1-Year structural target targets, chart projections, and sentiment maps.

Average 1Y Target
$8.82
▲ +9.16% Upside
Low Target
$4.00
-50% Risk
Median Target
$6.60
-18% Mid
High Target
$18.00
123% Max
Consensus
Buy
9 / 10 Buys

Consensus Trend Projection

Trailing closures vs. 12-month metrics map.

Analyst Vote Distribution

Aggregate institutional coverage sentiment weights.

📊 Historical Valuation Multiples

Real-time Trailing Twelve Month (TTM) momentum side-by-side with discrete quarterly metrics.

Fiscal QuarterTTMQ1 2026Q4 2025Q3 2025Q2 2025Q1 2025Q4 2024Q3 2024Q2 2024
Period EndingTrailing 12MMar 31, 2026Dec 31, 2025Sep 30, 2025Jun 30, 2025Mar 31, 2025Dec 31, 2024Sep 30, 2024Jun 30, 2024
Market Cap ($M)1,3959891,3031,446728837505425322
Enterprise Value ($M)1,3219151,2301,3929261,047705636534
Price to Earnings Ratio (P/E)114.12110.6929.38678.33-96.49-22.69-24.71-6.48-5.42
Price/Earnings-to-Growth Ratio (PEG)1.91170.81-5.08-681.70-2.30-0.50-0.30
Price to Sales Ratio (P/S)4.4311.9015.1819.4410.1813.928.417.826.70
Price to Book Ratio (P/B)105.9076.0295.17-1679.22-37.73-23.83-17.07-14.99-16.69
Price to Free Cash Flow Ratio (P/FCF)29.54103.6266.1080.02-7509.17-83.33287.99-50.60-29.96
Enterprise Value to Sales (EV/Sales)11.0014.3318.7212.9517.4211.7311.7311.11
Enterprise Value to EBITDA (EV/EBITDA)28.6374.1987.03125.69107.79852.80123.23-78.06-170.21
Debt to Equity Ratio-1.612.872.76-44.35-13.32-7.65-9.17-9.57-13.99

📘 Full Research Report

ℹ️

AI-Generated Research: This report is for informational purposes only.

📘 XERIS BIOPHARMA HOLDINGS INC (XERS) — Investment Overview

🧩 Business Model Overview

Xeris BioPharma commercializes and develops therapies for acute management of severe hypoglycemia, centered on glucagon rescue. The value chain runs from (1) product formulation and device integration (ready-to-use glucagon delivered via user-friendly systems) to (2) regulatory approval and manufacturing under cGMP quality standards, followed by (3) commercialization through payer contracting, specialty pharmacy distribution, and marketing/distribution support to endocrinology and diabetes-care channels. Demand is driven by diabetes prevalence and the clinical need for reliable emergency glucagon administration in patients and caregivers, where ease-of-use directly affects real-world outcomes and adherence to rescue plans.

💰 Revenue Streams & Monetisation Model

The revenue model is primarily product sales of glucagon rescue therapy, with monetization tied to unit volume, payer reimbursement dynamics, and product mix (for example, higher-value delivery formats can command stronger formulary positioning). Margin drivers include:

  • Gross margin stability influenced by manufacturing yields, cGMP overhead absorption, and component/device costs.
  • Net sales realization shaped by rebates/discounts, contract terms, and specialty distribution economics.
  • Mix effects depending on adoption of specific delivery systems and growth in covered patient populations.
  • Pipeline economics from potential additional products through development milestones, collaborations, or incremental commercial launches (if applicable to the portfolio strategy).

🧠 Competitive Advantages & Market Positioning

Xeris’ moat is best framed as a combination of Patent Protection and FDA/Regulatory Barriers to Entry, complemented by Intangible Assets in formulation stability and delivery usability that reduce “make-it-work” friction for patients and caregivers.

In severe hypoglycemia rescue, switching away from a familiar, easy-to-administer product can be constrained by clinical inertia, formulary coverage, and prescriber/caregiver comfort—creating partial switching-cost-like effects even without classic network economics.

  • Competitive benchmarking (primary peers): Eli Lilly (Baqsimi), Zealand Pharma / partners (Zegalogue), and Amphastar (legacy glucagon offerings and related rescue products).
  • Industry focus contrast: While competitors span multiple glucagon delivery modalities (nasal powder and alternative formulations/devices), Xeris focuses on ready-to-use glucagon designed to lower administration barriers during emergencies, targeting practical usability as a differentiator rather than relying solely on route-of-administration variety.

The durability of share depends on (1) label breadth and prescribing confidence, (2) formulary access and contracting, and (3) the continued strength of Xeris’ protected product architecture versus competitor launches and any next-generation rescue platforms.

🚀 Multi-Year Growth Drivers

Over a 5–10 year horizon, growth is supported by several secular and execution-oriented drivers:

  • Expanding diabetes prevalence increases the addressable population requiring emergency rescue planning.
  • Guideline and standard-of-care adoption supports ongoing prescribing of glucagon rescue products for at-risk patients and caregivers.
  • Payer formulary penetration can expand covered utilization when managed-care coverage broadens beyond initial access hurdles.
  • Label and indication refinement (when achieved through regulatory pathways) can increase eligible patient segments and reduce constraints to broader adoption.
  • Portfolio development through additional indications, next-generation devices, or adjacent therapies can extend revenue durability beyond a single product lifecycle.

⚠ Risk Factors to Monitor

  • Regulatory and IP risks: patent expirations, exclusivity challenges, and outcomes of patent disputes can compress pricing power and accelerate competition.
  • Competitive intensity: competing glucagon modalities can gain share through improved access, contracting strategies, or differentiated usability claims backed by payer/practice adoption.
  • Reimbursement and contracting: changes in rebate structures, specialty distribution economics, or payer utilization management can pressure net sales realization.
  • Manufacturing and supply chain: any cGMP quality issues or supply constraints can disrupt availability of emergency-rescue therapies.
  • Concentration risk: reliance on a limited number of commercial products increases sensitivity to volume shocks, competitive moves, and lifecycle events.
  • Clinical/portfolio execution: pipeline outcomes and commercialization readiness influence medium-term valuation and capital allocation credibility.

📊 Valuation & Market View

Equity market valuation for commercial biotech with a targeted product profile typically reflects a blend of (1) revenue durability, (2) gross margin trajectory, and (3) probability-adjusted pipeline optionality. Common framing metrics include EV/Revenue or P/S for revenue-generating assets, with deeper valuation shifts driven by:

  • Confidence in sustained demand and formulary access (net revenue realization quality).
  • Competitive positioning that protects share against alternative glucagon modalities.
  • Visibility into lifecycle management (product extensions, device evolution, and IP runway).
  • Pipeline credibility and the financial impact of new launches or partnered economics (when applicable).

🔍 Investment Takeaway

Xeris’ investment case rests on a defensible combination of regulatory/IP barriers and product usability advantages that matter materially in emergency hypoglycemia rescue. The core thesis is that diabetes prevalence and continued guideline-driven adoption can support durable product demand, while formulary access and patient/caregiver acceptance determine the pace of share capture versus glucagon peers such as Eli Lilly and Zealand Pharma. Key diligence centers on net sales durability, competitive contracting pressure, and the timeline of IP and regulatory protection.


⚠ AI-generated — informational only. Validate using filings before investing.

📰 Market News & Coverage

15 Stories Available

Real-time institutional reporting and market updates for XERS.

gurufocus.com2026-07-23

Xeris Biopharma to Report Second Quarter 2026 Financial Results on August 6, 2026

Xeris Biopharma Holdings, Inc. (Nasdaq: XERS), a fast-growing biopharmaceutical company committed to improving patient lives by developing and commercializing

businesswire.com2026-07-23

Xeris Biopharma to Report Second Quarter 2026 Financial Results on August 6, 2026

CHICAGO--(BUSINESS WIRE)--Xeris Biopharma Holdings, Inc. (Nasdaq: XERS), a fast-growing biopharmaceutical company committed to improving patient lives by developing and commercializing innovative products across a range of therapies, today announced that the Company will release its second quarter 2026 financial results before the open of the U.S. financial markets on Thursday, August 6, 2026. Management will host a conference call and webcast at 8:30 a.m. Eastern Time that day to discuss the C.

zacks.com2026-07-08

Xeris Biopharma (XERS) Moves 6.8% Higher: Will This Strength Last?

Xeris Biopharma (XERS) was a big mover last session on higher-than-average trading volume. The latest trend in earnings estimate revisions might not help the stock continue moving higher in the near term.

gurufocus.com2026-07-02

CORRECTING and REPLACING Xeris Announces Inducement Grants Under Nasdaq Listing Rule 5635(C)(4)

Please replace the release issued earlier today with the following corrected version that provides additional information regarding the inducement grants. Th

businesswire.com2026-07-02

CORRECTING and REPLACING Xeris Announces Inducement Grants Under Nasdaq Listing Rule 5635(C)(4)

CHICAGO--(BUSINESS WIRE)-- #GvokeHypoPen--Please replace the release issued earlier today with the following corrected version that provides additional information regarding the inducement grants. The corrected release reads: XERIS ANNOUNCES INDUCEMENT GRANTS UNDER NASDAQ LISTING RULE 5635(C)(4) Xeris Biopharma Holdings, Inc. (Nasdaq: XERS), a fast-growing biopharmaceutical company committed to improving patient lives by developing and commercializing innovative products across a range of therapies, today anno.

businesswire.com2026-07-02

Xeris Announces Inducement Grants Under Nasdaq Listing Rule 5635(C)(4)

CHICAGO--(BUSINESS WIRE)-- #GvokeHypoPen--Xeris Biopharma Holdings, Inc. (Nasdaq: XERS), a fast-growing biopharmaceutical company committed to improving patient lives by developing and commercializing innovative products across a range of therapies, today announced that on July 1, 2026, the Compensation Committee of Xeris' Board of Directors granted restricted stock units for an aggregate of 221,323 shares of its common stock to 47 new employees under Xeris' Inducement Equity Plan. Xeris' Inducement Equity Pla.

businesswire.com2026-06-30

Xeris Announces Updates to Its Board of Directors

CHICAGO--(BUSINESS WIRE)--Xeris Announces Updates to Its Board of Directors.

businesswire.com2026-06-11

Xeris Biopharma Announces Notice of Allowance From U.S. Patent and Trademark Office for New Patent Covering KEVEYIS®

CHICAGO--(BUSINESS WIRE)--Xeris Pharmaceuticals, Inc., a wholly owned subsidiary of Biopharma Holdings, Inc. (Nasdaq: XERS), a fast-growing biopharmaceutical company committed to improving patient lives by developing and commercializing innovative products across a range of therapies, announced that today the United States Patent and Trademark Office (USPTO) has issued a Notice of Allowance with respect to U.S. Patent Application No. 17/151,405, entitled “Compositions and Methods of Use.” The a.

gurufocus.com2026-06-11

Xeris Biopharma Announces Private Exchange of Convertible Notes

Xeris Biopharma Holdings, Inc. (Nasdaq: XERS), a fast-growing biopharmaceutical company committed to improving patient lives by developing and commercializing

businesswire.com2026-06-11

Xeris Biopharma Announces Private Exchange of Convertible Notes

CHICAGO--(BUSINESS WIRE)--Xeris Biopharma Holdings, Inc. (Nasdaq: XERS), a fast-growing biopharmaceutical company committed to improving patient lives by developing and commercializing innovative products across a range of therapies, today announced that it has entered into separate, privately negotiated exchange agreements with certain holders of its 8.00% Convertible Senior Notes due 2028 (the “Notes”). Pursuant to the exchange agreements, Xeris has agreed, subject to customary closing condit.

seekingalpha.com2026-05-30

Xeris Looks Ridiculously Cheap If Growth Forecasts Are Even Halfway Right

Xeris Biopharma has delivered another year of significant revenue growth, signaling a pivotal moment in its trajectory. XERS has reached an inflection point, indicating a shift in its business momentum and future prospects. The article highlights the company's expanding injectable medication portfolio as a driver for recent and anticipated growth.

marketbeat.com2026-05-09

Xeris Biopharma Q1 Earnings Call Highlights

Xeris Biopharma NASDAQ: XERS reported a sharp increase in first-quarter 2026 revenue and raised the low end of its full-year revenue outlook, citing strong demand for RECORLEV and continued execution across its commercial portfolio.

seekingalpha.com2026-05-07

Xeris Biopharma Holdings, Inc. (XERS) Q1 2026 Earnings Call Transcript

Xeris Biopharma Holdings, Inc. (XERS) Q1 2026 Earnings Call Transcript

zacks.com2026-05-07

Xeris Biopharma (XERS) Q1 Earnings: Taking a Look at Key Metrics Versus Estimates

The headline numbers for Xeris Biopharma (XERS) give insight into how the company performed in the quarter ended March 2026, but it may be worthwhile to compare some of its key metrics to Wall Street estimates and the year-ago actuals.

businesswire.com2026-05-07

Xeris Biopharma Reports First Quarter 2026 Financial Results

CHICAGO--(BUSINESS WIRE)--XERIS BIOPHARMA REPORTS FIRST QUARTER 2026 FINANCIAL RESULTS.

📊 AI Financial Analysis

Powered by StockMarketInfo
Earnings Data: Q Ending 2026-03-31

"XERS reported Q1’26 revenue of $83.13M and net income of $2.23M (EPS $0.01). QoQ, revenue declined from $85.81M in Q4’25 (−3.1%) while net income fell from $11.08M (−79.8%), indicating a sharp profitability normalization after a strong prior quarter. YoY, revenue rose from $60.12M in Q1’25 (+38.2%), and net income improved meaningfully from a net loss of $9.22M to a profit of $2.23M (turnaround). Over the 4-quarter window, margins shifted from deeply negative in Q1’25 (net margin −15.3%) to strong profitability in Q4’25 (net margin +12.9%) before contracting in Q1’26 to +2.7%. Operating income followed the same pattern: −$3.09M (Q1’25) → +$6.73M (Q3’25) → +$16.77M (Q4’25) → +$7.92M (Q1’26). Operating cash flow improved materially to $9.87M in Q1’26 (from −$10.03M in Q1’25 and $20.04M in Q4’25), and free cash flow was positive at $9.55M. Shareholder returns look strong given price momentum: the stock is up +56.1% over 1 year, with no dividend (dividend yield 0) and buybacks evident (Q1’26 common repurchases $17.0M). Balance sheet liquidity remains high (cash +ST investments $111.8M) with net cash (net debt −$74.4M). Overall, the quarter supports a continued YoY recovery, tempered by QoQ margin pressure."

Revenue Growth

Good

Revenue +38.2% YoY ($60.12M → $83.13M) but −3.1% QoQ ($85.81M → $83.13M), showing growth with recent cooling.

Profitability

Positive

Net income +$11.45M YoY turnaround (−$9.22M to +$2.23M). However QoQ net income fell −79.8% and net margin contracted from 12.9% (Q4’25) to 2.7% (Q1’26).

Cash Flow Quality

Positive

Operating cash flow was positive at $9.87M and free cash flow at $9.55M in Q1’26. Cash generation softened QoQ (from $20.04M OCF in Q4’25) but remains far above Q1’25.

Leverage & Balance Sheet

Good

Liquidity is strong with $111.8M cash/ST investments and net cash position (net debt −$74.4M). Total assets increased to $392.0M from $383.5M (Q4’25), indicating resilience.

Shareholder Returns

Strong

Total return signal is strong: 1Y price change +56.1%. No dividends (yield 0%), but buybacks are active (common repurchased $17.0M in Q1’26).

Analyst Sentiment & Valuation

Caution

Price is $6.37 versus consensus target $9 (upside ~41%). Valuation multiples appear elevated/unstable (e.g., P/E not meaningful across the loss-to-profit swing), suggesting higher risk despite targets.

Disclaimer:This analysis is AI-generated for informational purposes only. Accuracy is not guaranteed and this does not constitute financial advice.

Fundamentals Overview

Loading fundamentals overview...

Xeris reported a strong Q1 2026 with net product revenue up 43% to $82.5M and total revenue up 38% to $83.1M, led by Recorlev’s near-doubling (+95% to ~$50M) from record referrals and new patient starts. The company raised the low end of its 2026 revenue guidance to $380M–$390M (top end unchanged), citing early outperformance and confidence that momentum continues, with Recorlev’s completed commercial expansion expected to contribute incrementally in 2H 2026 and ramp over a typical 6–9 month period. Gross margin improved to 87% (+2% vs prior year) on favorable mix, while profitability improved meaningfully with adjusted EBITDA of $15.1M and net income of $2.2M. The primary near-term headwind was Gvoke, flat YoY due to Medicare resets increasing out-of-pocket costs and reducing prescription fills, not major formulary changes. XP-8121 remains on track for Phase III later in 2026, gated by go-to-market readiness.

AI IconGrowth Catalysts

  • Recorlev nearly doubled revenue to $50.0M (+95% YoY) driven by record referrals and record new patient starts, with continued momentum into April
  • Commercial expansion for Recorlev completed as planned; management expects incremental impact beginning in 2H 2026 and full ramp over 6–9 months after expansion
  • Revised full-year revenue outlook raised due to stronger-than-initial expectations, especially from Recorlev and Keveyis offsetting early Gvoke softness

Business Development

  • None explicitly disclosed in the call transcript (no named partners/customers/vendors provided)

AI IconFinancial Highlights

  • Q1 total revenue: $83.1M (+38% YoY); net product revenue: $82.5M (+43% YoY)
  • Recorlev net revenue: $49.8M (+95% YoY), +$24.2M vs Q1 prior year; driven by record referrals and record new patient starts
  • Gvoke net revenue: $20.8M (flat YoY), with softness attributed to Medicare policy/plan resets increasing deductibles and especially out-of-pocket costs, reducing filled prescriptions; no major formulary changes cited
  • Keveyis net revenue: $11.9M (+4% YoY), supported by modest net pricing and patient count improvements
  • Gross margin: 87% in Q1, up 2% vs prior year (increase attributed to favorable product mix)
  • R&D expense: $8.8M (+13% YoY) reflecting incremental XP-8121 program investment
  • SG&A: $53.1M (+21% YoY) driven by strategic Recorlev commercial expansion (nearly doubling Recorlev commercial team)
  • Adjusted EBITDA: $15.1M (+$10.7M vs prior year)
  • Net income: $2.2M (improved by >$11M vs prior year)
  • 2026 guidance raised: revenue now $380M–$390M (upward revision on low end); bottom-end raised from prior $375M to $380M while keeping top end at $390M

AI IconCapital Funding

  • No explicit buyback authorization/amount disclosed
  • No explicit ending cash/debt levels disclosed in the transcript
  • Management indicated capital allocation prioritizes reinvestment for growth, with debt/capital structure optionality as an available lever

AI IconStrategy & Ops

  • Recorlev commercial expansion completed; field infrastructure increased and management expects full productivity ramp over ~6–9 months, with the real drive expected in the back half of the year
  • Raised Recorlev field targets from ~7,000–8,000 to ~12,000 targets; now ~80 reps (plus expanded patient services/reimbursement and pharmacy capabilities)
  • Operational focus on scaling go-to-market readiness for XP-8121 prior to trial initiation (device, formulation, and commercial-scale formulation assembled and integrated before starting Phase III)
  • XP-8121 on track to begin Phase III later in 2026; management emphasized hosting a comprehensive program review later this fall to share Phase III trial design details

AI IconMarket Outlook

  • 2026 revenue guidance: $380M–$390M, representing >30% full-year revenue growth; low end raised to $380M
  • Gvoke expectation: modest growth in 2026 with first-quarter Medicare-reset softness expected to recover in subsequent quarters
  • Recorlev: expects impact from expanded infrastructure to begin incrementally in 2H 2026 and sustain thereafter

AI IconRisks & Headwinds

  • Gvoke near-term demand risk from Medicare resets: higher-than-normal out-of-pocket costs reduced number of patients getting prescriptions filled
  • Product adoption/tempo risk: management indicates it typically takes 6–9 months post-expansion for sales force to fully hit stride, implying near-term benefit timing uncertainty
  • Gvoke performance risk tied to channel-policy dynamics (Medicare noted as the primary driver in Q1)
  • Execution risk for XP-8121 Phase III readiness: trial start gated by go-to-market presentation readiness and scaling of device/formulation/commercial-scale processes

Q&A: Analyst Interest

  • Gvoke dynamics and whether formulary changes drove softness: Management said it was primarily standard Medicare payer reset effects—especially deductible and out-of-pocket cost increases—rather than meaningful formulary changes. They noted Medicare affected BAQSIMI too but felt channel mix differences explain relative impact versus competitors.
  • Recorlev growth mechanics and timing of commercial ramp: Management attributed momentum to typical payer resets followed by market testing/screening and diagnosis activity for hypercortisolemia. They stated the expanded field organization can capture more patients, but the real commercial expansion impact generally takes 6–9 months, pushing strongest benefits into the back half.
  • XP-8121 trial gating factors: Management said they will not start the trial until go-to-market commercial presentation readiness is in place. They described scaling up device and formulation—including commercial-scale formulation—then integrating these elements prior to initiating Phase III, and planned a full program review later this fall.

Sentiment: POSITIVE

Note: This summary was synthesized by AI from the XERS Q1 2026 earnings transcript. Financial data is complex; please verify all metrics against official SEC filings before making investment decisions.

📋 Official Regulatory 10-K / 10-Q SEC Filings

Direct authenticated documentation links to audited SEC database reports for XERS.

SEC EDGAR Live Feed
Loading financial data and tables...
📁

SEC Filings (XERS)

© 2026 Stock Market Info — Xeris Biopharma Holdings, Inc. (XERS) Financial Profile