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Cormedix Therapeutics Reports First Quarter 2026 Financial Results and Provides Business Update

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(Positive)
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CorMedix Therapeutics (Nasdaq:CRMD) reported Q1 2026 net revenue of $127.4 million, net income of $38.6 million, and adjusted EBITDA of $70.0 million. DefenCath generated $97.5 million, including a non-recurring $9.0 million benefit, while the Melinta portfolio contributed $29.9 million.

The company raised 2026 net revenue guidance to $325–$345 million and adjusted EBITDA guidance to $115–$135 million. Positive Phase III topline results for REZZAYO in prophylaxis support an sNDA filing targeted for the second half of 2026. Cash and short-term investments totaled $178.1 million.

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AI-generated analysis. Not financial advice.

Positive

  • Q1 2026 net revenue $127.4 million, up from $39.1 million in Q1 2025
  • Q1 2026 net income $38.6 million; basic EPS $0.48, diluted $0.43
  • Q1 2026 adjusted EBITDA $70.0 million versus $23.6 million a year earlier
  • Raised 2026 net revenue guidance to $325–$345 million
  • Raised 2026 adjusted EBITDA guidance to $115–$135 million
  • Positive Phase III topline results for REZZAYO prophylaxis program
  • Cash and short-term investments of $178.1 million at March 31, 2026

Negative

  • Q1 2026 operating expenses $41.5 million, up about 139% year over year
  • Selling and marketing expense rose to $12.5 million from $4.5 million
  • G&A expense increased to $21.7 million from $9.7 million
  • Q1 DefenCath revenue benefited from a non-recurring $9.0 million sales allowance adjustment
  • DefenCath growth described in context of pending TDAPA expiration, implying future reimbursement uncertainty

News Market Reaction – CRMD

+5.73%
26 alerts
+5.73% News Effect
+13.8% Peak in 57 min
+$32M Valuation Impact
$588.32M Market Cap
0.2x Rel. Volume

On the day this news was published, CRMD gained 5.73%, reflecting a notable positive market reaction. Argus tracked a peak move of +13.8% during that session. Our momentum scanner triggered 26 alerts that day, indicating elevated trading interest and price volatility. This price movement added approximately $32M to the company's valuation, bringing the market cap to $588.32M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Q1 2026 net revenue: $127.4 million Q1 2026 net income: $38.6 million Q1 2026 adjusted EBITDA: $70.0 million +5 more
8 metrics
Q1 2026 net revenue $127.4 million First quarter 2026 net revenue
Q1 2026 net income $38.6 million First quarter 2026 net income
Q1 2026 adjusted EBITDA $70.0 million First quarter 2026 adjusted EBITDA
DefenCath net revenue $97.5 million Q1 2026 DefenCath sales contribution
Favorable change in estimate $9.0 million Non-recurring change in sales allowance estimate for DefenCath
Melinta portfolio revenue $29.9 million Q1 2026 acquired Melinta portfolio revenue
2026 revenue guidance $325–$345 million Updated full-year 2026 net revenue guidance range
2026 adj. EBITDA guidance $115–$135 million Updated full-year 2026 adjusted EBITDA guidance range

Market Reality Check

Price: $8.45 Vol: Volume 917,048 is slightl...
normal vol
$8.45 Last Close
Volume Volume 917,048 is slightly below the 20-day average of 992,536 (relative volume 0.92). normal
Technical Shares trade below the 200-day MA, with price at 7.545 versus MA(200) of 9.7, and about 56.71% under the 52-week high.

Peers on Argus

Pre-news, CRMD was roughly flat (-0.13%) while key biotech peers were mixed: ABU...
1 Down

Pre-news, CRMD was roughly flat (-0.13%) while key biotech peers were mixed: ABUS -4.01%, MRVI -6.22%, QURE +0.59%, UPB +4.46%, VERV -0.09%. Only ABUS appeared on the momentum scanner, moving down.

Previous Earnings Reports

5 past events · Latest: Mar 05 (Positive)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Mar 05 Q4 & full-year earnings Positive -11.5% Reported strong Q4 and 2025 results with high revenue, net income and EBITDA.
Jan 08 Prelim FY25 results Positive -32.8% Issued preliminary Q4/FY25 results and introduced upbeat 2026 revenue and EBITDA guidance.
Nov 12 Partner earnings update Neutral -1.8% Talphera Q3 update including CorMedix-led financing and NEPHRO CRRT study progress.
Nov 12 Q3 2025 earnings Positive +2.1% Reported strong Q3 revenue, high EBITDA and raised 2025 pro forma guidance and synergies.
Oct 20 Prelim Q3 2025 Positive +19.4% Announced preliminary Q3 beat with higher DefenCath sales and raised 2025 guidance and synergies.
Pattern Detected

Earnings-related headlines have often been followed by negative moves despite generally strong fundamentals and raised guidance, though there are instances of positive alignment when guidance was increased.

Recent Company History

Over the past few quarters, CorMedix used earnings updates to highlight rapid growth from DefenCath and the Melinta acquisition, frequently raising revenue and adjusted EBITDA guidance. Prior earnings and preliminary results (e.g., Oct 20, 2025 and Nov 12, 2025) emphasized higher pro forma revenue, strong EBITDA and synergy capture, yet average post‑earnings moves have been negative. Today’s Q1 2026 beat‑and‑raise update fits this pattern of strong reported fundamentals and expanded outlook.

Historical Comparison

-4.9% avg move · In the last five earnings‑tagged releases, CRMD’s average move was about -4.92%, often selling off a...
earnings
-4.9%
Average Historical Move earnings

In the last five earnings‑tagged releases, CRMD’s average move was about -4.92%, often selling off after strong revenue and guidance. Today’s Q1 2026 beat‑and‑raise fits that pattern of fundamentally solid but market‑skeptical earnings reactions.

Earnings updates show a progression from strong Q3 2025 results and rising pro forma guidance to robust Q4/FY25 performance, followed by reaffirmed and then raised 2026 revenue and adjusted EBITDA guidance as Melinta integration and DefenCath growth scale.

Regulatory & Risk Context

Active S-3 Shelf
Shelf Active
Active S-3 Shelf Registration 2025-10-07

An effective S-3ASR filed on 2025-10-07 registers up to 6,323,833 existing shares for resale by Deerfield-affiliated securityholders. The prospectus states CorMedix will receive no proceeds from these sales and lists $140,000 of related legal fees and expenses.

Market Pulse Summary

The stock moved +5.7% in the session following this news. A strong positive reaction aligns with Cor...
Analysis

The stock moved +5.7% in the session following this news. A strong positive reaction aligns with CorMedix’s delivery of Q1 2026 net revenue of $127.4M, net income of $38.6M, and adjusted EBITDA of $70.0M, alongside higher 2026 guidance of $325–$345M in revenue. Historically, earnings strength sometimes met skepticism, so any outsized upside could be sensitive to profit‑taking, the non‑recurring $9.0M benefit, and future execution on REZZAYO and TPN trials.

Key Terms

adjusted EBITDA, phase iii, snda, allogeneic hematopoietic stem cell transplantation, +2 more
6 terms
adjusted EBITDA financial
"Net Income of $38.6 million; Adjusted EBITDA of $70.0 million"
Adjusted EBITDA is a way companies measure how much money they make from their core operations, like running a business, by removing certain costs or income that aren’t part of regular business activities. It helps investors see how well a company is doing without distractions from unusual expenses or gains, making it easier to compare companies or track performance over time.
phase iii medical
"positive Phase III topline results from the global ReSPECT clinical trial"
A Phase III trial is the late-stage clinical study that tests whether a medical treatment works and is safe in a large group of patients, often comparing it to standard care. Think of it as a final dress rehearsal or full-scale road test before regulators decide on approval; positive or negative results strongly influence a drug maker’s chance to sell the treatment, future revenue, and investment risk.
snda regulatory
"prepare for FDA submission of the sNDA, expected in the second half of this year"
A SNDA (Subordination, Non‑Disturbance and Attornment Agreement) is a legal pact among a property owner’s lender, the owner’s tenants, and sometimes the landlord that sets who keeps lease rights if the property is sold or a mortgage is enforced. Think of it as a rulebook that decides whether a tenant can stay and keep paying rent or must answer to a new owner after a foreclosure. For investors, an SNDA matters because it protects predictable rental income, clarifies who has priority on claims against a property, and therefore affects a property’s value and the security of related loans.
allogeneic hematopoietic stem cell transplantation medical
"in adult patients undergoing allogeneic hematopoietic stem cell transplantation"
A procedure in which blood-forming stem cells are taken from a healthy donor and given to a patient to replace a diseased or damaged blood and immune system, similar to swapping out a failing factory’s machinery so it can produce healthy products again. Investors care because it underpins markets for related drugs, medical devices and hospital services, and outcomes — including success rates, complications and regulatory approvals — can materially affect company value and healthcare costs.
catheter lock solution medical
"Phase 3 study of taurolidine/heparin catheter lock solution in TPN patients"
A catheter lock solution is a sterile liquid placed inside an indwelling catheter between uses to prevent blood clots and bacterial growth, much like a protective cap that keeps a tool clean and ready. Investors care because the product’s safety, effectiveness and regulatory approval affect hospital purchasing, recurring revenue from supplies, and liability or reimbursement risks tied to patient outcomes and healthcare costs.
total parenteral nutrition medical
"catheter lock solution in TPN patients continues to enroll patients"
Total parenteral nutrition is a medical treatment that supplies all needed calories, fluids, vitamins and minerals directly into a patient’s bloodstream through an IV, bypassing the digestive tract — like a complete meal delivered by a drip. It matters to investors because TPN relies on specialized ingredients, preparation and delivery services with steady hospital and home-care demand, significant regulation and reimbursement exposure, and potential for durable revenue or risk from supply-chain or clinical issues.

AI-generated analysis. Not financial advice.

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‒ Q1 2026 Net Revenue of $127.4 million

‒ Q1 2026 Net Income of $38.6 million; Adjusted EBITDA of $70.0 million

Company raises FY 2026 Revenue and Adjusted EBITDA Guidance

‒ Conference Call Scheduled for Today at 8:30 a.m. Eastern Time ‒

PARSIPPANY, N.J., May 14, 2026 (GLOBE NEWSWIRE) -- CorMedix Therapeutics (Nasdaq: CRMD) today announced financial results for the first quarter ended March 31, 2026 and provided an update on its business.

Recent Corporate Highlights:

  • CorMedix announces $127.4 million of net revenue for the first quarter of 2026, reflecting strong first quarter execution and positive underlying demand trends. The Company also recognized net income of $38.6 million and adjusted EBITDA of $70.0 million.(1) Basic and fully diluted EPS were $0.48 and $0.43 per share, respectively, for the quarter.

  • DefenCath® (taurolidine and heparin) sales contributed $97.5 million of net revenue in the quarter, bolstered by higher utilization of DefenCath by outpatient dialysis customers as well as a non-recurring $9.0 million favorable change in estimate related to certain sales allowances. The acquired Melinta portfolio contributed $29.9 million, reflecting typical, first quarter purchasing patterns for the anti-infective portfolio.

  • CorMedix updates previously established guidance for 2026 net revenue and adjusted EBITDA. The Company increases full-year 2026 net revenue guidance to a range of $325 to $345 million, and full-year adjusted EBITDA guidance to a range of $115 to $135 million.

  • On April 27, 2026, CorMedix announced positive Phase III topline results from the global ReSPECT clinical trial evaluating REZZAYO® (rezafungin for injection) for prophylaxis of invasive fungal diseases in adult patients undergoing allogeneic hematopoietic stem cell transplantation. CorMedix is actively working together with its global partner to prepare for FDA submission of the sNDA, expected in the second half of this year, and targeting for a potential commercial launch for the expanded indication in 2027.

  • The ongoing Phase 3 study of taurolidine/heparin catheter lock solution in TPN patients continues to enroll patients and is currently trending to completion in 2028. The Company is taking appropriate steps to accelerate enrollment trajectory, including the opening of new study sites and the submission of a protocol amendment to FDA, which, if approved, would remove certain exclusion criteria and broaden patient enrollment.

  • Cash and short-term investments, excluding restricted cash, at March 31, 2026 totaled $178.1 million.

Joseph Todisco, CorMedix Chairman & CEO, commented, “CorMedix has entered 2026 with strong momentum across all areas of our business. DefenCath continues to exceed expectations despite pending TDAPA expiration and demonstrates strong underlying utilization demand. In addition, we are advancing a pipeline of late-stage opportunities, including REZZAYO for prophylaxis, which we expect will meaningfully expand our long-term revenue opportunity. Lastly, we have delivered significant profitability and cash generation, allowing us to reinvest in growth, as well as shareholder value creation through stock repurchases, while preserving financial flexibility for new business development initiatives."

(1) Adjusted EBITDA is a non-GAAP financial measure and excludes non-cash items such as depreciation, amortization, stock-based compensation, interest and other income and expense, taxes and certain non-recurring items. See “Non-GAAP Financial Measures” on the following pages for additional information regarding the use of EBITDA and Adjusted EBITDA and a reconciliation to the most comparable GAAP measure.

First Quarter 2026 Financial Highlights

For the first quarter of 2026, CorMedix recorded $127.4 million in net revenue, comprised of $97.5 million in sales of DefenCath and $29.9 million in revenue associated with the acquired Melinta portfolio, an increase from $39.1 million in net revenue in the comparable period of 2025. DefenCath sales in the quarter were positively impacted by a non-recurring $9.0 million change in estimate related to certain sales allowances. DefenCath sales increased year over year largely due to the onboarding of a large dialysis organization in mid-2025. As the Melinta acquisition occurred in August 2025, the first quarter of 2025 included net revenue from only sales of DefenCath.

Total operating expenses in the first quarter of 2026 were $41.5 million, compared with $17.4 million in the first quarter of 2025, an increase of approximately 139%. The increase of $24.1 million over the prior period was driven primarily by the contribution of operating expenses from the Melinta acquisition for the full quarter and reflects the larger combined company.

Research and development (R&D) expenses in the first quarter of 2026 were $7.2 million, compared with $3.2 million for the same period in 2025. The increase in R&D was primarily due to an increase in personnel and clinical trial services in support of the ongoing clinical programs, including pediatric studies for several of our brands and the continued investment in the development of DefenCath for the TPN indication.

Selling and marketing expense increased approximately 180% to $12.5 million in first quarter of 2026 from $4.5 million in the first quarter of 2025. The increase was primarily due to higher personnel cost associated with the larger product portfolio and related marketing programs.

General and administrative expenses increased approximately 124% to $21.7 million in the first quarter of 2026 from $9.7 million in the first quarter of 2025. The increase was primarily attributable to higher costs associated with operating as a combined company following the acquisition, including higher personnel, information technology, branded prescription drug, legal and facilities costs.

CorMedix recorded net income of $38.6 million, or $0.48 and $0.43 per basic and diluted share, respectively, in the first quarter of 2026, compared with net income of $20.6 million, or $0.32 and $0.30 per basic and diluted share, respectively, in the first quarter of 2025. Also for the first quarter of 2026, CorMedix reported adjusted EBITDA of $70.0 million, compared to adjusted EBITDA of $23.6 million in the first quarter of 2025.

The Company reported cash and cash equivalents of $178.1 million at March 31, 2026, excluding restricted cash. The Company believes that it has sufficient resources to fund operations for at least twelve months from the issuance of the Company’s Quarterly Report on Form 10-Q.

Conference Call Information

The management team of CorMedix will host a conference call and webcast today, May 14, 2026, at 8:30AM Eastern Time, to discuss recent corporate developments and financial results. Call details and dial-in information are as follows:

May 14, 2026 @ 8:30am ET

Domestic:1-844-676-2922
International:1-412-634-6840
Webcast:Webcast Link
  

About CorMedix

CorMedix Therapeutics is a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of life-threatening conditions and diseases in the United States. CorMedix is focused on selling and marketing products in institutional settings of care in the US and has field based medical and commercial infrastructure deployed in hospitals, clinics and infusion centers. For more information visit: www.cormedix.com.

Forward-Looking Statements

This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, as amended (the “Exchange Act”), that are subject to risks and uncertainties. Forward-looking statements are often identified by the use of words such as, but not limited to, “anticipate,” “believe,” “can,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “project,” “seek,” “should,” “target,” “will,” “would,” and similar expressions or variations intended to identify forward-looking statements. All statements, other than statements of historical facts, regarding management’s expectations, beliefs, goals, plans or CorMedix’s prospects should be considered forward-looking statements including, but not limited to statements regarding financial and business guidance; sales, revenue and operating expense estimates; synergy estimates and timing; accretion estimates; Adjusted EBITDA estimates; the risk that topline data from CorMedix’s and its partners’ clinical trials, including the ReSPECT study, that CorMedix announces or publishes from time to time may change as more patient data become available or may be interpreted differently if additional data is disclosed; estimates of total addressable market size; expectations regarding product utilization and sales; failure to successfully conduct future clinical trials, including due to CorMedix’s or its partners’ potential inability to enroll or retain sufficient patients to conduct and complete the trials or generate data necessary for regulatory approval, among other things; development of unexpected safety or efficacy concerns related to CorMedix’s product candidates; expectations and timing regarding clinical trials and development and expectations of CorMedix’s product pipeline; expectations regarding implementation and perceived benefits of CorMedix’s products; continued pricing pressures and the impact of actions of governmental and private payers affecting pricing of, reimbursement for, and patient access to pharmaceuticals; and reporting obligations related thereto, the expiration of intellectual property protection for certain of the company's products and competition from generic and biosimilar products. Readers are cautioned that actual results may differ materially from projections or estimates due to a variety of important factors, and readers are directed to the Risk Factors identified in CorMedix’s filings with the SEC, including its most recent Annual Report on Form 10-K, copies of which are available free of charge at the SEC’s website at www.sec.gov or upon request from CorMedix. CorMedix may not actually achieve the goals or plans described in its forward-looking statements, and such forward-looking statements speak only as of the date of this press release. In addition, pro forma financial information does not necessarily reflect the actual results that we would have achieved had the pro forma transaction been consummated as of the date indicated nor does it reflect the potential future results of the combined company. Investors should not place undue reliance on these statements. CorMedix assumes no obligation and does not intend to update these forward-looking statements, except as required by law.

Non-GAAP Financial Measures

This release includes certain non-GAAP financial measures, including EBITDA and adjusted EBITDA, which are intended as supplemental measures of the Company’s performance that are not required by or presented in accordance with GAAP. Management uses these non-GAAP measures internally to evaluate and manage the Company’s operations and to better understand its business because they facilitate a comparative assessment of the Company’s operating performance relative to its performance based on results calculated under GAAP. These non-GAAP measures also isolate the effects of some items that vary from period to period without any correlation to core operating performance and eliminate certain charges that management believes do not reflect the Company’s operations and underlying operational performance.

The Company believes that these non-GAAP measures also provide useful information to investors regarding certain financial and business trends relating to the Company’s financial condition and operating results, which facilitates an evaluation of the financial performance of the Company and its operations on a consistent basis. Providing this information therefore allows investors to make independent assessments of the Company’s financial performance, results of operations and trends while viewing the information through the eyes of management.

These non-GAAP measures are subject to limitations. The non-GAAP measures presented in this release may not be comparable to similarly titled measures used by other companies because other companies may not calculate one or more in the same manner. Additionally, the non-GAAP performance measures exclude significant expenses and income that are required by GAAP to be recorded in the Company’s financial statements; do not reflect changes in, or cash requirements for, working capital needs. Further, our historical adjusted results are not intended to project our adjusted results of operations or financial position for any future period. To compensate for these limitations, management presents and considers these non-GAAP measures in conjunction with the Company’s GAAP results; no non-GAAP measure should be considered in isolation from or as alternatives to any measure determined in accordance with GAAP. Readers should review the reconciliations included below, and should not rely on any single financial measure to evaluate the Company’s business.

Investor Contact:
Dan Ferry
Managing Director
LifeSci Advisors
daniel@lifesciadvisors.com
(617) 430-7576

   
CORMEDIX INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(In Thousands, Except Per Share Data)
(Unaudited)
   
  For the Three Months Ended
March 31,
  2026   2025
Revenue:     
Product sales, net$121,916  $39,082
Contract revenue 5,511   -
Total Revenue$127,427  $39,082
Cost of sales (exclusive of amortization of intangibles)$12,005  $1,545
Amortization of intangibles 10,300   52
Gross profit$105,122  $37,485
Operating Expenses:     
Research and development$7,212  $3,193
Selling and marketing 12,532   4,474
General and administrative 21,720   9,693
Total Operating Expenses$41,464  $17,360
Income From Operations$63,658  $20,125
Other (Expense) Income:     
Unrealized loss on marketable security$(3,546) $-
Change in contingent consideration (4,199)  -
Other non-operating (expense) income, net (268)  519
Total Other (Expense) Income$(8,013) $519
Income before income taxes$55,645  $20,644
Tax expense 17,044   
Net Income$38,601  $20,644
Net Income Per Common Share – Basic$0.48  $0.32
Net Income Per Common Share - Diluted$0.43  $0.30
Weighted Average Common Shares Outstanding – Basic 79,509   65,244
Weighted Average Common Shares Outstanding – Diluted 92,985   68,975


       
CORMEDIX INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED BALANCE SHEET DATA
(In Thousands)
       
  March 31   December 31,
  2026   2025
  (Unaudited)   (Audited)
       
ASSETS      
Cash and cash equivalents$178,087  $144,837
Short-term investments$  $3,694
Trade receivables, net$154,807  $171,233
Inventories$30,731  $29,716
Goodwill and intangible assets$398,774  $409,074
Deferred tax assets$3,312  $16,276
Other current and long-term assets$49,926  $51,312
Total Assets$815,637  $826,142
       
Total Liabilities$378,588  $420,835
Stockholders' Equity$437,049  $405,307
Total Liabilities and Stockholders’ Equity$815,637  $826,142


   
CORMEDIX INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(In Thousands)
(Unaudited)
   
  For the Three Months Ended
March 31,
  2026
(Unaudited)
  2025
(Unaudited)
      
Cash Flows from Operating Activities:     
Net income$38,601  $20,644 
Net cash provided by (used in) operating activities$42,382  $19,737 
Net cash (used in) provided by investing activities$2,965  $(195)
Net cash provided by financing activities$(12,097) $6,093 
Net Increase (Decrease) in Cash and Cash Equivalents$33,250  $25,635 
Cash, Cash Equivalents and Restricted Cash - Beginning of Period$145,825  $40,756 
Cash, Cash Equivalents and Restricted Cash - End of Period$179,075  $66,391 


 
CORMEDIX INC. AND SUBSIDIARIES
Non-GAAP Reconciliations
(In Thousands)
(Unaudited)
 
  For the Three Months Ended
March 31,
  2026   2025 
Net income$38,601  $20,644 
Adjusted to add (deduct):     
Interest (income) expense, net 182   (557)
Provision for income taxes 17,044    
Depreciation and amortization 10,544   162 
EBITDA (Non-GAAP)$66,371  $20,249 
Adjusted to add (deduct):     
Change in estimate for sales allowances (8,983)   
Stock-based compensation expense 4,582   3,500 
Merger-related and reorganization costs 183   (146)
Other (income) expense 7,831   38 
Adjusted EBITDA (Non-GAAP)$69,984  $23,641 

FAQ

What were CorMedix (CRMD) Q1 2026 earnings and revenue results?

CorMedix reported Q1 2026 net revenue of $127.4 million and net income of $38.6 million. According to CorMedix, adjusted EBITDA reached $70.0 million, with basic and diluted EPS of $0.48 and $0.43 per share, respectively, reflecting higher product sales and portfolio expansion.

How did DefenCath sales impact CorMedix (CRMD) Q1 2026 performance?

DefenCath generated $97.5 million of Q1 2026 net revenue, significantly shaping overall results. According to CorMedix, sales benefited from higher outpatient dialysis utilization and a non-recurring $9.0 million favorable change in sales allowance estimates, plus contributions from a large dialysis organization onboarded in mid-2025.

Did CorMedix (CRMD) raise its full-year 2026 guidance after Q1 results?

CorMedix increased its 2026 net revenue guidance to $325–$345 million and adjusted EBITDA guidance to $115–$135 million. According to CorMedix, the higher outlook reflects Q1 performance, demand for DefenCath, and contributions from the acquired Melinta anti-infective portfolio.

What were the Phase III REZZAYO trial results announced by CorMedix (CRMD)?

CorMedix announced positive Phase III topline results from the global ReSPECT trial of REZZAYO for prophylaxis in allogeneic stem cell transplant patients. According to CorMedix, it plans an sNDA submission in the second half of 2026 and is targeting a potential commercial launch for the expanded indication in 2027.

What is the status of CorMedix (CRMD) taurolidine/heparin TPN Phase 3 trial?

The Phase 3 study of taurolidine/heparin catheter lock solution in TPN patients is ongoing and trending to completion in 2028. According to CorMedix, actions to accelerate enrollment include opening new sites and proposing a protocol amendment to broaden patient eligibility criteria.

How strong is CorMedix (CRMD) cash position after Q1 2026?

CorMedix reported $178.1 million in cash and short-term investments, excluding restricted cash, as of March 31, 2026. According to CorMedix, this balance is expected to fund operations for at least twelve months from the issuance of its Quarterly Report on Form 10-Q.

What were the main drivers of higher operating expenses for CorMedix (CRMD) in Q1 2026?

Total operating expenses rose to $41.5 million in Q1 2026 from $17.4 million a year earlier. According to CorMedix, the increase reflects full-quarter Melinta-related costs, higher R&D for clinical programs, and larger selling, marketing, and general and administrative expenses for the combined company.