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CRMDNasdaq

CorMedix Inc.

Pharmaceutical preparations·Commercial·Parsippany, NJ, United States·CEO: Mr. Joseph Todisco MBA
Infectious DiseaseNephrology

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BioSniper AI · CRMD

CorMedix Inc. is a commercial-stage biopharmaceutical company focused on developing and commercializing therapies for the prevention of catheter-related bloodstream infections, with its lead product DefenCath (taurolidine and heparin) approved and launched in the U.S. dialysis market.

Key risk: Commercial adoption dependence

7.2/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$646.9M

Cash Runway

Financial data as of Jun 30, 2026.

Tracking 2 pipeline candidates · 3 clinical trials · 3 catalysts · 1 FDA decision for CorMedix Inc..

AI OverviewAI overview is shown in English only.

CorMedix Inc. is a commercial-stage biopharmaceutical company focused on developing and commercializing therapies for the prevention of catheter-related bloodstream infections, with its lead product DefenCath (taurolidine and heparin) approved and launched in the U.S. dialysis market.

  • Reported total revenue of $101.9M and net income of $26.0M for the six months ended June 30, 2026 [sec].
  • Cash and equivalents of $257.7M as of June 30, 2026, with shareholders' equity of $220.6M [sec].
  • DefenCath is approved and commercialized in the U.S. under a Transitional Drug Add-on Payment Adjustment (TDAPA) program that provides five years of additional reimbursement beyond the ESRD bundled rate [sec_mda · as of 2024-05-09].
  • The company has multi-year commercial supply agreements covering roughly 60% of U.S. outpatient dialysis centers [sec_mda · as of 2025-03-25].
  • A Phase 3 topline readout is expected on January 1, 2028, and patent/exclusivity expiries for REZZAYO and DEFENCATH are scheduled for 2038 and 2042, respectively [upcoming catalysts].

What works

  • DefenCath has secured broad commercial coverage with contracts representing about 60% of U.S. outpatient dialysis centers, providing a large addressable patient base [sec_mda · as of 2025-03-25].
  • The TDAPA program offers five years of additional reimbursement beyond the standard ESRD bundled rate, supporting revenue growth during the early commercial phase [sec_mda · as of 2024-05-09].
  • The company achieved profitability with net income of $26.0M in the first half of 2026, indicating improving operating leverage [sec].
  • A strong cash position of $257.7M as of June 30, 2026 provides financial flexibility to fund operations and development activities [sec].

What to weigh

  • Revenue and profitability remain dependent on successful continued adoption of DefenCath; failure to maintain or expand market penetration could reverse recent financial improvements [sec_mda · as of 2025-03-25].
  • The company faces risks from reimbursement dynamics and the timing of product adoption, which could affect revenue predictability [sec_mda · as of 2026-08-13].
  • Clinical development of pipeline candidates is subject to uncertainties in enrollment, costs, and timelines, with no guarantee of successful outcomes [sec_mda · as of 2026-03-05].
  • Future capital needs may require dilutive equity or debt financing, as the company has an ATM program and shelf registration available for additional securities issuance [sec_mda · as of 2025-08-07].

From the filings

Quoted directly from source documents.

  • DefenCath has commercial supply agreements covering roughly 60% of U.S. outpatient dialysis centers.

    We believe the currently contracted customer base represents roughly 60% of the outpatient dialysis centers in the U.S.

    SEC MD&A · March 25, 2025

  • The TDAPA program provides five years of additional reimbursement for DefenCath.

    The TDAPA program currently provides for five years of additional payment reimbursement beyond the ESRD bundled rate to outpatient providers.

    SEC MD&A · May 9, 2024

Catalyst timeline

  • 2028-01-01 · Phase3_ToplineTopline results from a Phase 3 adaptive study will provide key efficacy and safety data for a pipeline candidate.
  • 2038-07-14 · Patent_Expiry · REZZAYOPatent/exclusivity expiry for REZZAYO may open the product to generic competition.
  • 2042-04-15 · Patent_Expiry · DEFENCATHPatent/exclusivity expiry for DEFENCATH may open the product to generic competition.
Risks & what to watch (4)

Key risks

  • Commercial adoption dependenceRevenue growth relies on continued adoption of DefenCath; failure to maintain market penetration could reverse profitability [sec_mda · as of 2025-03-25].
  • Reimbursement and pricing uncertaintyChanges in reimbursement dynamics or TDAPA program terms could materially affect revenue [sec_mda · as of 2026-08-13].
  • Clinical development risksPipeline candidates face uncertainties in enrollment, costs, and outcomes; no guarantee of successful development [sec_mda · as of 2026-03-05].
  • Potential dilutive financingFuture capital needs may require equity or debt issuance, diluting existing shareholders [sec_mda · as of 2025-08-07].

What to watch

  • Continued commercial adoption of DefenCath and its impact on revenue growth and profitability [sec_mda · as of 2026-08-13].
  • Phase 3 topline data readout expected on January 1, 2028, which could inform pipeline value [upcoming catalysts].
  • Reimbursement dynamics under the TDAPA program and any changes to the ESRD bundled payment system [sec_mda · as of 2024-05-09].
  • Capital allocation decisions, including potential use of the ATM program or shelf registration for additional funding [sec_mda · as of 2025-08-07].

Sources: SEC MD&A · Generated August 29, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash Runway10.0

Profitable (positive operating cash flow)

Financial Health6.8

D/E 0.96 · 18% dilution

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth4.6

2 candidates

Catalyst Momentum6.0

3 upcoming, next in ~489d

Insider SignalN/A

No insider transactions in the last 180 days

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

189

Total value held

$307.7M

Showing top 10 of 189 institutional holders of CorMedix Inc.. Open the full 13F history after sign-in.

Short Interest

as of May 20, 2026
% of float
21.0%
Days to cover
16.0
Shares short
16,222,947
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

CRMD short interest

Governance

Frequently asked questions

What is the AI investment thesis for CorMedix Inc.?

CorMedix Inc. is a commercial-stage biopharmaceutical company focused on developing and commercializing therapies for the prevention of catheter-related bloodstream infections, with its lead product DefenCath (taurolidine and heparin) approved and launched in the U.S. dialysis market.

What is CorMedix Inc.'s lead drug candidate?

CorMedix Inc.'s most advanced tracked candidate is DefenCath (Phase 4) for reduction of central line associated bloodstream infection (CLABSI) in adult patients receiving total parental nutrition (TPN).

What is CorMedix Inc.'s next catalyst?

CorMedix Inc.'s next tracked catalyst is a Phase3_Topline event — "Phase 3 Topline: A Phase 3, Prospective, Multicenter, Double-Blind, Randomized, Controlled, Adaptive Study To Demonst" — expected January 1, 2028.

Who is the CEO of CorMedix Inc.?

Mr. Joseph Todisco MBA is the chief executive officer of CorMedix Inc. (CRMD).

Where is CorMedix Inc. headquartered?

CorMedix Inc. (CRMD) is headquartered in Parsippany, NJ, United States.

925 companies232,681 SEC filings21,419 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.