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NCT07421024Active, not recruitingPhase 2

GRK-Biased Activation Via β2-Adrenergic Receptors in Human Skeletal Muscle

G Protein-Coupled Receptor Kinase (GRK)-Biased Signaling Via β2-Adrenergic Receptors and Downstream Activation and Its Role for Protein Synthesis-Regulating Kinases, Function and Receptor Desensitization in Human Skeletal Muscle

Source: ClinicalTrials.gov · Last updated 14 Oct 2026

Brief summary (registry, in English)

This longitudinal mechanistic physiological study examines biased β2-adrenergic receptor (β2-AR) signaling in human skeletal muscle, with emphasis on G protein-coupled receptor kinase (GRK)-mediated pathways. Participants will receive daily oral dosing of the GRK-selective long-acting β2-agonist ATR-258 for 8 weeks. Muscle biopsies and physiological measurements will quantify GRK-, cAMP/PKA-, and β-arrestin-related up- and downstream signaling, fiber-type specificity, and potential receptor desensitization with repeated stimulation along with functional read-outs, tissue distribution, cardiovascular response and tolerability.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
13 (actual)
First submitted
30 Jan 2026
Start date
19 Feb 2026
Primary completion date
31 Dec 2026
Lead sponsor
Morten Hostrup, PhD
Diseases
Obesity
NCT number
NCT07421024

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 13
  • From 19 Feb 2026 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Regular use of or allergy to β2-agonists
  • Regular use of medication (except OTC allergy or analgesics)
  • Hypertension
  • Cardiovascular, metabolic, gastrointestinal, renal, or pulmonary disease
  • Psychiatric or neurological disorders affecting compliance/safety reporting
  • Cancer history within the last 5 years

Lab values

  • Reduced kidney function (eGFR \< 90 ml/min/1.73m\^2)

Other

  • Serious adverse reactions to β2-agonists
  • Current smoker
  • Abnormal ECG before or after β2-AR stimulation
  • Substance abuse or alcohol intake \>14 units/week

Who the study is looking for

  • Healthy men
  • Age 21-45 years
  • BMI 25-35 kg/m\^2
  • Body fat percentage 25-40%
  • Lean Mass Index 14-22

Age in the registry: 21 years to 45 years · Sex: Male · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Copenhagen, August Krogh Section for Human & Molecular Physiology
Coordinator of this site? Confirm its status
CopenhagenDenmarkUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.