FDA Approves Phraxis' EndoForce™ Connector for Dialysis Access

Analysis reveals significant industry trends and economic implications

Release Date

2025-05-23

Category

Drug Approval Event

Reference

Source

Breakthrough Clinical Results

Phraxis Inc. announced FDA approval of its EndoForce™ Connector for Endovascular Venous Anastomosis, a medical device designed to simplify the creation of arteriovenous grafts (AVGs) for hemodialysis. The device uses a minimally invasive approach, eliminating the need for surgical dissection and promoting precise vessel-to-graft alignment. A pivotal study demonstrated a 92% patency rate at six months. The EndoForce™ Connector is now available to healthcare providers, offering a potentially improved solution for patients with end-stage renal disease (ESRD).

Key Highlights

  • FDA approval of EndoForce™ Connector for Endovascular Venous Anastomosis.
  • Minimally invasive approach eliminates surgical dissection for AVG creation.
  • 92% patency rate at six months in a pivotal study.
  • Improved procedural efficiency and reduced complications.

Incidence and Prevalence

Global Estimates of End-stage Renal Disease (ESRD) Incidence and Prevalence

Chronic kidney disease is a rising global epidemic with a worldwide prevalence of 11-13%, which can potentially lead to End-stage renal disease (ESRD).

Regional Data

Puerto Rico (2000-2008)

United States

Pakistan

Risk Factors and Comorbidities

Risk Factors and Comorbidities for End-Stage Renal Disease (ESRD)

Top Risk Factors for ESRD

  1. Diabetes mellitus:

  2. Type 2 diabetes mellitus is a leading cause of ESRD

  3. The world is experiencing an "epidemic of Type 2 DM" contributing to increased ESRD cases

  4. Diabetic nephropathy has increased in absolute numbers and as a proportion of patients with ESRD

  5. Diabetes as a cause of ESRD (particularly if insulin-dependent) is associated with increased mortality risk

  6. Diabetic nephropathy accounts for a significant percentage of all incident ESRD cases

  7. Hypertension/Cardiovascular disease:

  8. Hypertensive nephrosclerosis is a significant risk factor

  9. Hypertension is identified as the major cause of renal disease presentation at 53.93%

  10. In black patients with hypertensive nephrosclerosis, increased proteinuria and reduced GFR are directly associated with adverse clinical renal events

  11. Proteinuria:

  12. Baseline proteinuria is consistently associated with increased risk for adverse renal outcomes

  13. This relationship is evident even at low levels of proteinuria

  14. Proteinuria remains a risk factor even when stratified by level of GFR

Top Comorbidities for ESRD

  1. Cardiovascular disease:

  2. Coronary artery disease and congestive heart failure, each present in 41% of ESRD patients

  3. Cardiovascular disease starts early in renal insufficiency and may worsen with renal replacement therapy

  4. Accounts for more than 50% of ESRD deaths

  5. Cardiovascular mortality in ESRD is particularly high after acute myocardial infarction and in patients with other forms of atherosclerotic vascular disease

  6. Left ventricular hypertrophy and dysfunction:

  7. Two major determinants are anemia and hypertension

  8. Anemia:

  9. Very common in ESRD patients

  10. A major determinant of left ventricular hypertrophy

Additional Risk Factors

  • Hyperuricemia - associated with increased risk of developing ESRD, particularly in women
  • Reduced GFR (especially levels <40 ml/min)
  • Age - older age is associated with increased mortality risk
  • Abnormal laboratory values - elevated serum creatinine, urea nitrogen, and phosphorus
  • Low serum albumin - 50% of patients had serum albumin <3.5 gm/dl at onset of ESRD with increased mortality risk
  • Malnutrition - undernourished patients had elevated risk (RR = 1.34)
  • History of neoplasm
  • Active smoking
  • Low serum creatinine concentration
  • Chronic glomerulonephritis

Drug used in other indications

Based on the provided context, there is no information available about the EndoForce™ Connector device, its clinical trials, or any intervention models being used in such trials. The context materials focus on various aspects of End-Stage Renal Disease (ESRD) treatment including dialysis options, medications, and clinical trial endpoints, but do not contain any references to the specific connector device in question.

The available information covers topics related to ESRD such as: - Epidemiology and treatment modalities - Genetic factors in ESRD development - Valve surgery in ESRD patients - Diabetes as a cause of ESRD - Cardiovascular disease in ESRD patients - Bioengineering approaches for ESRD - Self-management support interventions - TAVR outcomes in ESRD patients - Technology-assisted cognitive-behavioral therapy for ESRD patients

However, none of these materials mention the EndoForce™ Connector device, its applications for ESRD, or any alternative indications for which it might be being trialed.

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