Three-Year Efficacy and Safety of Lebrikizumab in Patients with Moderate-to-Severe Atopic Dermatitis: A Long-Term Extension (ADjoin) - Scorecard - MDSpire

Three-Year Efficacy and Safety of Lebrikizumab in Patients with Moderate-to-Severe Atopic Dermatitis: A Long-Term Extension (ADjoin)

  • By

  • Emma Guttman-Yassky

  • Alan D. Irvine

  • Melinda Gooderham

  • Stephan Weidinger

  • Lynda Spelman

  • Jonathan I. Silverberg

  • Heidi Crane

  • Hany ElMaraghy

  • Louise DeLuca-Carter

  • Maria Lucia Buziqui Piruzeli

  • Georgia Martimianaki

  • Evangeline Pierce

  • Helena Agell

  • Diamant Thaçi

  • June 19, 2026

  • 0 min

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Clinical Scorecard: Long-Term Efficacy and Safety of Lebrikizumab in Moderate-to-Severe Atopic Dermatitis Patients: Results from a Three-Year Extension Study (ADjoin)

At a Glance

CategoryDetail
ConditionAtopic Dermatitis (AD)
Key MechanismsLebrikizumab is a monoclonal antibody that binds to interleukin (IL)-13, blocking its downstream effects.
Target PopulationAdults and adolescents 12 years and older with moderate-to-severe AD.
Care SettingClinical trials and long-term treatment settings.

Key Highlights

  • Lebrikizumab demonstrated durable improvement in AD symptoms through 3 years.
  • Safety profile consistent with previously reported data.
  • Long-term treatment supports disease control and quality of life improvement.

Guideline-Based Recommendations

Diagnosis

  • Diagnosis of moderate-to-severe AD based on clinical criteria.

Management

  • Lebrikizumab is recommended as a treatment option for moderate-to-severe AD.

Monitoring & Follow-up

  • Monitor for efficacy and safety during long-term treatment.

Risks

  • Potential for uncontrolled AD in patients not achieving sustained long-term clinical benefit.

Patient & Prescribing Data

Patients with moderate-to-severe AD who have previously completed specific studies.

Lebrikizumab is effective for long-term management of AD symptoms.

Clinical Best Practices

  • Consider lebrikizumab for patients who have not achieved adequate control with other therapies.
  • Assess patient response at week 16 to determine eligibility for continued treatment.

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