The Effects of ATLAS Therapy on Nitric Oxide Bioavailability in Patients With Intermittent Claudication

Last updated: April 2, 2025
Sponsor: Louis Messina
Overall Status: Active - Recruiting

Phase

1

Condition

Intermittent Claudication

Vascular Diseases

Peripheral Arterial Occlusive Disease

Treatment

L-Ascorbate

Tetrahydrobiopterin 10 mg/kg

Tetrahydrobiopterin 20 mg/kg

Clinical Study ID

NCT04800692
H00012734
  • Ages > 18
  • All Genders

Study Summary

This study will focus on people with claudication from peripheral arterial disease. The investigators are researching whether a multicomponent therapeutic can increase the production of Nitric Oxide in the blood and whether that leads to an improvement in pain free walking distance and overall physical activity.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • PAD as demonstrated by an ABI <0 .9 in one leg or TBI less than <0.7 in patientswith an ABI >1.3 (non compressible vessels)

  • Rutherford Classification II, III

  • Age >18 years old

  • Willingness to discontinue phosphodiesterase (PDE) 5 inhibitors such as Viagra,Cialis, Levitra, Revatio

  • Willingness to discontinue phosphodiesterase (PDE) 3inhibitors cilostazol, milrinoneor Vesnarinone

  • Willing and able to comply with all study procedures

  • Willing and able to provide informed consent

  • Sexually active subjects willing to use an acceptable method of contraception whileparticipating in the study

Exclusion

Exclusion Criteria:

  • Hypotension defined as a systolic blood pressure less than 100mmhg systolic atscreening or baseline visit

  • Critical Leg Ischemia (Rutherford Classification IV, V, VI)

  • Surgical intervention to alleviate symptoms of claudication in the study leg withinthe past 6 months or any endovascular interventions within 3 months or who isscheduled to undergo surgical revascularization in the next 6 month

  • Walking limited by reasons other than claudication (e.g. arthritis, lung disease,severe neuropathy, lower extremity amputation except single digits)

  • Serum creatinine >1.5mg/dl or Hepatic enzymes >2X the upper limit of normal

  • Serum potassium greater than 5.0 or use of a potassium sparing diuretic at screening

  • Pregnant, breast feeding or planning to become pregnant (subject or partner) at anytime during the study.

  • Myocardial Infarction, Cerebrovascular Accident or deep vein thrombosis within 12months of screening

  • Known history of nephrolithiasis

  • History of ever having a seizure

  • Concurrent disease or condition that would interfere with study participation orsafety such as bleeding disorders, organ transplant, long term immunosuppression (excluding inhaled steroids), current neoplasm or severe gastroesophageal reflux

  • History of vertigo or syncope within the past 10 years

  • Enrollment in another drug or device study within 30 days of screening

  • Required treatment with a drug known to inhibit folate metabolism (e.g.Methotrexate)

  • Taking any of the following medications; PDE3 Inhibitors, PDE5 inhibitors, trental,nitrates, ginkgo biloba, levodopa, warfarin,

  • Axillary lymph node dissection

  • Presence of an amputation except single digits in either leg

  • Preexisting illness that limits ambulation such as severe COPD, class III-IV heartfailure, severe arthritis or back pain

  • Glucose-6-dehydrogenase deficiency

Study Design

Total Participants: 10
Treatment Group(s): 4
Primary Treatment: L-Ascorbate
Phase: 1
Study Start date:
June 15, 2021
Estimated Completion Date:
December 31, 2027

Study Description

The primary objective of this study is to show that ATLAS Therapy, (L-Arginine; Tetrahydrobiopterin; L-Ascorbate) is bioavailable in humans and exerts a measurable effect on its in vivo biological signature, Flow Mediated Vasodilation (FMD) in people with intermittent claudication caused by peripheral arterial disease. This will be a Phase I / dose finding study. All subjects will receive 2 different drug doses of the Kuvan the first 45 days they will receive 10 mg/kg/day. The second 45 days they will receive 20/mg/kg/day.

Connect with a study center

  • UMASS Memorial Healthcare - University Campus

    Worcester, Massachusetts 01655
    United States

    Active - Recruiting

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