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A Study of LY3471851 in Participants With Eczema

Nektar Therapeutics logo

Nektar Therapeutics

Status and phase

Completed
Phase 1

Conditions

Dermatitis, Atopic

Treatments

Drug: LY3471851
Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT04081350
17240
J1P-MC-KFAD (Other Identifier)

Details and patient eligibility

About

The main purpose of this study is to learn more about the safety and side effects of LY3471851 when given by injection just under the skin to participants with eczema. The study will last up to 48 weeks and may include up to 23 visits to the study center.

Enrollment

48 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Have a confirmed diagnosis of atopic dermatitis (AD) for least 12 months
  • Have active AD according to study specific criteria
  • Be willing and able to undergo skin biopsies

Exclusion criteria

  • Have received certain topical medications for AD within 14 days prior to baseline
  • Have received certain systemic medications for AD within 4 weeks prior to baseline
  • Have received LY3471851 previously

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

48 participants in 4 patient groups, including a placebo group

10 µg/kg LY3471851
Active Comparator group
Description:
Participants received subcutaneous (SC) injection of 10 microgram per kilogram (μg/kg) LY3471851 every 2 weeks for a treatment period of 12 weeks.
Treatment:
Drug: LY3471851
12 µg/kg LY3471851
Active Comparator group
Description:
Participants received subcutaneous injection of 12 μg/kg LY3471851 every 2 weeks for a treatment period of 12 weeks.
Treatment:
Drug: LY3471851
24 µg/kg LY3471851
Active Comparator group
Description:
Participants received subcutaneous injection of 24 μg/kg LY3471851 every 2 weeks for a treatment period of 12 weeks.
Treatment:
Drug: LY3471851
Placebo
Placebo Comparator group
Description:
Participants received subcutaneous injection of placebo every 2 weeks for a treatment period of 12 weeks.
Treatment:
Drug: Placebo

Trial contacts and locations

20

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Data sourced from clinicaltrials.gov

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