key: cord-0029524-dwcdronh
authors: Sidbury, Robert; Alpizar, Sady; Laquer, Vivian; Dhawan, Sunil; Abramovits, William; Loprete, Luca; Krishnaswamy, Jayendar Kumar; Ahmad, Faiz; Jabbar-Lopez, Zarif; Piketty, Christophe
title: Pharmacokinetics, Safety, Efficacy, and Biomarker Profiles During Nemolizumab Treatment of Atopic Dermatitis in Adolescents
date: 2022-01-28
journal: Dermatol Ther (Heidelb)
DOI: 10.1007/s13555-021-00678-7
sha: a7b8913b2724f7a41f6f7055a300ba9a64a497ff
doc_id: 29524
cord_uid: dwcdronh

INTRODUCTION: Nemolizumab, a new monoclonal antibody that targets the receptor alpha of the neuroimmune cytokine interleukin-31 (IL-31), has shown efficacy in atopic dermatitis (AD) in adults. This study evaluated the pharmacokinetics (PK) and safety of nemolizumab in adolescents with moderate to severe AD as well as the relationship between nemolizumab concentrations and clinical efficacy and the effect of nemolizumab on protein biomarkers. METHODS: Open-label, 16-week study of nemolizumab in patients aged 12–17 years with moderate to severe AD (baseline EASI ≥ 16, IGA ≥ 3, and BSA ≥ 10%) and associated pruritus with baseline average daily peak pruritus numeric rating scale (PP-NRS) intensity of at least 4. Nemolizumab was administered subcutaneously as a loading dose of 60 mg at baseline, followed by 30 mg every 4 weeks until week 12 with background topical corticosteroids (TCS) or calcineurin inhibitors (TCI). Subsequently patients were followed for 8 weeks more. Stratum corneum (SC) and plasma samples were collected for biomarker assessments. RESULTS: Twenty patients participated, with a mean age of 14.8 ± 1.6 years. The PK of nemolizumab was described by a one-compartment model with linear elimination, a first-order absorption, and a mean half-life of 16.7 ± 4.1 days. Mean trough concentrations ranged from 2935 ± 1029 ng/mL to 3292 ± 2018 ng/mL over the 16-week treatment period. There was a marked improvement in rash, itch, and sleep with a decrease from baseline to week 16 in EASI by 66.5 ± 32.5%, in PP-NRS by 43.2 ± 37%, and in sleep disturbance numeric rating scale by 53.5 ± 47.8%. The popPK and PK/PD analyses confirmed that model-predicted exposure and efficacy of nemolizumab were similar in adolescents compared to adults receiving the same dosing regimens. Age did not impact PK parameters, while the main source of PK variability was body weight. Analyses of SC samples identified a panel of AD-related pro-inflammatory biomarkers that were upregulated in lesional skin (compared to non-lesional skin) and correspondingly downregulated in clinical responders to nemolizumab (based on EASI75 and PP-NRS ≥ 4). Four biomarkers (CCL20, CCL22, CCL27, and VEGF) had changes that were 1.9–3.5-fold higher in EASI responders than in EASI non-responders (all p < 0.05). Analysis showed no significant correlation between plasma biomarkers and clinical scores. Adverse events were experienced by 33.3% of subjects (n = 6) and were primarily mild or moderate in severity. CONCLUSIONS: Nemolizumab PK and safety profiles in adolescents with moderate to severe AD are consistent with previous nemolizumab studies in adults. PK/PD models demonstrate similar exposure–response profiles in 12- to 17-year-old adolescents and adults for three clinical endpoints (EASI, IGA, and PP-NRS). Nemolizumab treatment reversed AD-related pro-inflammatory biomarkers in skin, indicating that the neuroimmune cytokine IL-31 is an important mediator of multiple pathways in AD. CLINICAL TRIAL REGISTRATION: Clinicaltrials.gov NCT03921411. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13555-021-00678-7.

numeric rating scale (PP-NRS) intensity of at least 4. Nemolizumab was administered subcutaneously as a loading dose of 60 mg at baseline, followed by 30 mg every 4 weeks until week 12 with background topical corticosteroids (TCS) or calcineurin inhibitors (TCI). Subsequently patients were followed for 8 weeks more. Stratum corneum (SC) and plasma samples were collected for biomarker assessments. Results: Twenty patients participated, with a mean age of 14.8 ± 1.6 years. The PK of nemolizumab was described by a one-compartment model with linear elimination, a first-order absorption, and a mean half-life of 16.7 ± 4.1 days. Mean trough concentrations ranged from 2935 ± 1029 ng/mL to 3292 ± 2018 ng/mL over the 16-week treatment period. There was a marked improvement in rash, itch, and sleep with a decrease from baseline to week 16 in EASI by 66.5 ± 32.5%, in PP-NRS by 43.2 ± 37%, and in sleep disturbance numeric rating scale by 53.5 ± 47.8%. The popPK and PK/PD analyses confirmed that model-predicted exposure and efficacy of nemolizumab were similar in adolescents compared to adults receiving the same dosing regimens. Age did not impact PK parameters, while the main source of PK variability was body weight. Analyses of SC samples identified a panel of AD-related pro-inflammatory biomarkers that were upregulated in lesional skin (compared to non-lesional skin) and correspondingly downregulated in clinical responders to nemolizumab (based on EASI75 and PP-NRS C 4). Four biomarkers (CCL20, CCL22, CCL27, and VEGF) had changes that were 1.9-3.5-fold higher in EASI responders than in EASI non-responders (all p \ 0.05). Analysis showed no significant correlation between plasma biomarkers and clinical scores. Adverse events were experienced by 33.3% of subjects (n = 6) and were primarily mild or moderate in severity. Conclusions: Nemolizumab PK and safety profiles in adolescents with moderate to severe AD are consistent with previous nemolizumab studies in adults. PK/PD models demonstrate similar exposure-response profiles in 12-to 17-year-old adolescents and adults for three clinical endpoints (EASI, IGA, and PP-NRS). Nemolizumab treatment reversed AD-related pro-inflammatory biomarkers in skin, indicating that the neuroimmune cytokine IL-31 is an important mediator of multiple pathways in AD. Clinical Trial Registration: Clinicaltrials.gov NCT03921411.

Keywords: Nemolizumab; Atopic dermatitis; Biomarkers; Pharmacokinetics; Adolescents

Nemolizumab, a monoclonal antibody that targets the receptor alpha of the neuroimmune cytokine IL-31, has shown efficacy in atopic dermatitis (AD) in adults.

This study evaluated the pharmacokinetics (PK) and safety of nemolizumab in adolescents with AD and the effect of nemolizumab on protein biomarkers.

Nemolizumab PK and safety profiles in adolescents with moderate to severe AD are consistent with previous nemolizumab studies in adults and nemolizumab treatment reversed AD-related proinflammatory biomarkers in skin, indicating that the neuroimmune cytokine IL-31 is an important mediator of multiple pathways in AD.

Atopic dermatitis (AD) is a common inflammatory skin disease, affecting 10-20% of the population and as many as 25% of children [1] [2] [3] . Chronic pruritus can be considered a diseasedefining symptom of AD; additional characteristic signs and symptoms include xerosis, and eczematous lesions that may manifest as erythema, infiltration/papulation, oozing/crusting, excoriations, and lichenification [3, 4] . Notably, approximately 30% of children and 50% of adult patients with AD have moderate to severe disease [5] [6] [7] . Topical treatment with corticosteroids or calcineurin inhibitors can be efficacious, especially in milder AD [4] ; proactive therapy with topical corticosteroid (TCS) and tacrolimus is recommended by recent guidelines for therapy of AD [8] . However, topical therapy may not always be sufficient to control moderate to severe AD [9] . Systemic immunosuppressive treatments such as cyclosporine, methotrexate, mycophenylate or azathioprine are more efficacious, but are often accompanied by adverse effects [4] . In recent years, knowledge of the pathophysiologic factors in AD has increased, and a variety of new treatments have either received regulatory approval or are undergoing clinical evaluation for efficacy and safety, including nemolizumab [4] . The first drug approved by the US Food and Drug Administration (FDA) for treatment of moderate to severe AD was dupilumab in December 2020. Dupilumab is approved for adolescents with moderate to severe AD eligible for systemic therapy and can currently be considered as a first-choice systemic treatment in this population [10, 11] .

Nemolizumab, a new monoclonal antibody that targets the receptor alpha of the neuroimmune cytokine interleukin-31 (IL-31), has shown efficacy in AD in adults [12] [13] [14] . In phase 2 studies of adults with moderate to severe AD, nemolizumab improved AD lesions and pruritus with a favorable safety profile [15] [16] [17] . AD is most common in childhood but there are limited data with nemolizumab in patients aged younger than 18. The primary objective of this study was to evaluate the pharmacokinetics (PK) and safety of nemolizumab in adolescents with moderate to severe AD. Secondary objectives were to evaluate the relationship between nemolizumab systemic exposure and clinical efficacy endpoints (pharmacokinetic/pharmacodynamic relationship) and the effect of nemolizumab therapy on protein biomarkers as an exploratory endpoint.

This was an open-label, 16-week study of nemolizumab in patients aged 12-17 years with moderate to severe AD and associated pruritus not adequately controlled with topical therapy. Nemolizumab was administered subcutaneously as a loading dose of 60 mg at baseline, followed by 30 mg every 4 weeks until week 12 with background TCS treatment; the treatment period ended at week 16 and patients were followed for an additional 8 weeks. Additional details on the study methodology are provided in the Supplementary Material.

Ethics committee approval was provided by ADVARRA, 6940 Columbia Gateway Drive Suite#110, Columbia, MD 21046 USA. This study was conducted in accordance with the accepted version of the Declaration of Helsinki and all relevant federal regulations as set forth in Parts 50, 56, 312, Subpart D, of Title 21 of the US Code of Federal Regulations, in compliance with International Council for Harmonization (ICH) Good Clinical Practice (GCP) guidelines, and according to the appropriate regulatory requirements in the countries where the study was conducted. Before any study procedures were performed, each subject (or their legally acceptable representative[s] if applicable) voluntarily signed and dated the informed consent form (ICF, or assent form, as applicable).

In addition to inadequate response to topical AD medications, the following disease-severity criteria were required for eligibility: baseline Eczema Area and Severity Index (EASI) score C 16, Investigator Global Assessment (IGA) score of 3 or higher, and AD body surface area (BSA) involvement of at least 10%; AD-associated pruritus was indicated by a baseline average daily peak pruritus numeric rating scale (PP-NRS) intensity of at least 4. The primary exclusion criteria were body weight \ 30 kg, poorly controlled asthma or current history of chronic obstructive pulmonary disease and/or chronic bronchitis, and history of failure on another biologic or JAK inhibitor.

Rescue therapy could be prescribed to subjects at any time during the study (except the run-in period) as deemed necessary by the investigator. As a general guideline, rescue therapy was not prescribed within the first 2 weeks after baseline to allow assessment of study drug exposure. Rescue therapy was directed at AD, and included topical calcineurin inhibitors, higher potency TCS, oral corticosteroids, biologics, phototherapy, or systemic nonsteroidal immunosuppressants/immunomodulators. If rescue therapy was topical or phototherapy, study drug administration continued; study drug was permanently discontinued if systemic rescue was required.

The primary objective of the study was to evaluate the safety and pharmacokinetics of nemolizumab; however, efficacy assessments were performed including EASI scoring, IGA scores (0 = none to 4 = severe, with treatment success defined as a score of 0/1 or clear/almost clear), BSA, and the SCORing Atopic Dermatitis (SCORAD) measure. Changes in itch and sleep were also captured, using the PP-NRS and a sleep disturbance NRS (SD-NRS), both scales from 0 = none to 10 = worst imaginable. Safety evaluations were conducted at every visit and included collection of adverse events, physical examination, and laboratory assessments.

Blood samples to determine the PK profile of nemolizumab were collected. Serum concentration was assessed at baseline, weeks 1-2, 4, 8, 12, 16, and 24, and determined using a validated enzyme-linked immunosorbent assay (ELISA) method with a quantification limit of 100 ng/mL (Shin Nippon Biomedical Laboratories, Japan).

A first-order absorption and one-compartment distribution population PK (popPK) model was initially developed using nemolizumab serum concentrations from three clinical studies conducted in 407 adults. The studies assessed nemolizumab administered subcutaneously over the dose range of 0.1-3 mg/kg and 10-90 mg for weight-based and flat dosing, respectively. The effect of several covariates including age, body weight, serum creatinine, estimated glomerular filtration rate, bilirubin, serum albumin, total protein, IgE, sex, and clinical study was explored. The final model identified in the adult population was used to derive individual empirical Bayes estimates of model-derived PK parameters in the adolescent population, including maximum/trough concentrations (C max , C trough ), area under the curve (AUC), volume of distribution (V d /F), oral clearance (CL/F), and absorption rate (k a ).

Three pharmacokinetic/pharmacodynamic (PK/PD) models were developed to correlate the concentration of nemolizumab to clinical efficacy. The PK/PD models were applied to the following PD endpoints: EASI, IGA, and weekly average PP-NRS.

Serum samples to assess anti-drug antibodies (ADA) were assessed at baseline, weeks 4, 8, 12, 16, and 24, and determined using a validated electrochemiluminescence immunoassay (ECLIA) method (LSI Medience Corporation, Japan).

The effect of nemolizumab was investigated on 30 selected biomarkers relevant to AD on both plasma and stratum corneum (SC) samples [15] . Plasma samples were collected at baseline and weeks 8 and 16. Samples of the SC were collected at baseline and week 16 via tape strips (D-Squame). Two lesional and two non-lesional areas were identified at baseline and four tape strips were collected from each area (16 total). At week 16, samples were collected only from the two lesional areas identified at baseline (eight strips in total). Levels of proteins were associated with clinical parameters (75% response on EASI [EASI75], IGA B 1, PP-NRS decrease by at least 4 points).

All efficacy analyses used the intent-to-treat (ITT) population which included all enrolled subjects who signed a consent form; all safety data were summarized using the safety population which included all subjects who were administered at least one dose of study medication; all pharmacokinetic analyses were performed using the PK population including all subjects who provided at least one post-baseline evaluable drug concentration value. Subject disposition, demographics, baseline characteristics, previous therapies, and concomitant therapies were summarized by descriptive statistics. Efficacy variables were summarized by analysis visit from baseline unless specified otherwise. Efficacy analyses were performed using last observation carried forward (LOCF) or non-responder imputation. Efficacy data after use of rescue medication were treated as treatment failure and were set to missing for analysis. Adverse events were summarized using the number and percentage of subjects reporting each system organ class and preferred term. Changes in physical examination were summarized by body system and visit from baseline. Changes in laboratory assessments were summarized by descriptive statistics by visit.

Nemolizumab serum concentration data (in nanograms per milliliter) were summarized by visit from baseline to week 24 using the following statistics: n, arithmetic mean, standard deviation, %CV, geometric mean, %CV geometric mean, median, minimum, maximum, 95% CI of mean and number of BLQs (below limit of quantification). Estimates of popPK parameters (Cl/F, V d /F, k a ), including inter-individual variability, IIV), covariate effects, residual error and their relative standard error (RSE) were presented. Individual derived PK parameters at steady state were summarized using the following statistics: n, arithmetic mean, SD, geometric mean, %CV, median, minimum, maximum and 95% CI. All pharmacokinetic analyses were based on the observed cases, and no missing data were imputed.

Primary inference for all biomarker analyses was based on the observed cases. All biomarker variables (e.g., absolute and change from baseline) were summarized descriptively at each time point. In addition, a box plot was produced at each time point. If the variable did not have a Gaussian distribution, it was log transformed.

A total of 20 subjects were enrolled (ITT population), of which 18 subjects were treated at least once and were included in the safety and PK populations. Two subjects who did not meet inclusion criteria and were enrolled in error received no doses of nemolizumab. Thirteen subjects received all treatment doses (completers), and five subjects discontinued early (three because of adverse events and two because of protocol deviations).

Demographic and disease characteristic information are presented in Table 1 . Subjects in the ITT population had a mean age of 14.8 ± 1.6 years and body weights ranging from 49 to 112 kg. Ten subjects (50.0%) had a medical history of stable asthma at baseline.

Peak nemolizumab serum concentrations were observed either at week 1 or week 2 visits after Fig. 1 , average nemolizumab observed exposures in adolescents were comparable to those in adults receiving the same dosing regimens. A population pharmacokinetic (popPK) model developed from adult data was used to describe the time course of nemolizumab exposure and investigate sources of variability in the PK profile of nemolizumab (details of the model are provided in the Supplementary Material). The pharmacokinetics of nemolizumab were described by a one-compartment model with linear elimination, a first-order absorption, and a lag time. A moderate impact of the dose was identified on the bioavailability with an increase of bioavailability with decreasing dose. Body weight was confirmed as the main source of PK variability, impacting both elimination (CL/F) and distribution (V/F), with increasing body weight translating to decreased systemic exposure. The albumin plasma concentrations moderately impacted CL/F. Estimates of the main population PK parameters in adults are reported in Table 2 .

The adult model was then used to predict the nemolizumab individual PK profile in Fig. 1 Average predicted and observed nemolizumab concentrations in adolescents and adults NC not calculated, CL/F apparent clearance after extravascular administration, V d /F apparent volume of distribution after extravascular administration, k a firstorder constant of absorption, t 1/2 terminal half-life, C max maximum drug concentration, AUC inf area under the concentration-time curve to infinity adolescents using their baseline characteristics (age, body weight, albumin levels) and dosing history and then compared to the observed data. As shown in Table 2 and Fig. 1 , the popPK model developed from adult data was able to accurately predict nemolizumab PK in adolescents. No impact of age was observed on estimates for systemic clearance, volume of distribution, constant of absorption, or terminal half-life obtained with popPK modeling.

Overall incidence of ADA formation in the adolescent population was limited, as only 1 of 18 subjects presented treatment-related ADA at week 4. No ADA-positive sample had neutralizing antibodies. Importantly, serum nemolizumab concentrations in ADA-positive subjects were not different from those in ADA-negative subjects.

There was an improvement in AD signs and symptoms in subjects treated with nemolizumab. The mean EASI score was reduced from 25.2 ± 7.2 at baseline to 8.0 ± 9.0 at week 16, a 66.5% (32.5) improvement (Fig. 2 ). In addition, 9/15 (60%) of subjects had a 75% response on EASI (EASI75) score at week 16. Improvement in the mean IGA was observed beginning at week 4 and continued to increase through week 16. By week 16, seven subjects (35%) achieved IGA success (0/1 or clear/almost clear plus C 2 grade improvement). The mean SCORAD scores were reduced from 63.0 at baseline to 30.0 at week 16, a 50% reduction. Concomitantly, there was a -53% reduction in mean BSA involvement from baseline to week 16, from 41.3% at baseline to 19.4% at week 16. Improvements in pruritus were indicated by PP-NRS and SD-NRS. There was an improvement in PP-NRS by 43.2 ± 37% (from 6.9 at baseline to 3.8 at week 16). By week 16, 5/10 (50%) of subjects were judged PP-NRS responders, defined as a weekly improvement in PP-NRS score C 4 points. Better quality sleep was demonstrated by a mean -53.5% change from baseline in SD-NRS.

PK/PD analyses showed that model-predicted efficacy (described by IGA, EASI, and PP-NRS clinical assessments) was similar in adolescents compared to adults (details of the modeling are provided in the Supplementary Material).

Supervised and unsupervised analyses (see Supplemental Methods) on 30 AD-relevant biomarkers were performed. In the supervised analysis, six proteins were identified that were significantly associated with EASI75 response: CCL18, CCL20, CCL22, CCL27, IL1RA with false discovery rate (FDR) \ 0.05, and VEGF-A with FDR \ 0.10, where the FDR considered is the minimum adjusted p value (interaction, main effect). Four of these biomarkers (CCL20, CCL22, CCL27, and VEGF) had changes that were 1.9-3.5-fold higher in EASI responders Fig. 2 Percentage change from baseline in EASI score at each study visit. ITT population than in EASI non-responders (all p \ 0.05, Fig. 3 ). Although not significant from an FDR criterion, CCL17 was also significantly different between lesional and non-lesional skin in EASI75 responders and was concomitantly reduced post-treatment in week 16 lesional skin. Further, CCL17 and CCL20 expression in the SC were significantly associated with PP-NRS (Fig. 4) . Finally, unsupervised analysis identified 15 proteins (including the six proteins found by the supervised analyses) that were significantly associated with EASI75 (p = 0.0041; Fig. 5 ). These included CCL18, CCL20, CCL22, CCL27, CX3CL1, CXCL6, CXCL8, CYSTATIN, FASL, GALECTIN, IL-11, IL-21, IL-1RA, SPD, VEGF-A (Fig. 5) . Biomarker analysis showed no significant correlation between the measured proteins in plasma and clinical scores (data not shown).

Adverse events were experienced by 33.3% of subjects (n = 6) and were primarily mild or moderate in severity. There were no deaths and three serious adverse events occurred in two The p value corresponds to the interaction between sample type and EASI75 responders (Y; blue line) vs non responders (N; red line). Least-square estimated means (LS means) are shown with 95% confidence intervals for each treatment in each skin condition (lesional/non lesional baseline and week 16). For simplicity, only the interaction p value is mentioned in the figure, but the selection criterion is based on the minimum adjusted p value (interaction, main effect) subjects (eczema, peripheral edema, and staphylococcal skin infection); those two subjects discontinued the study. There were four adverse events of special interest, which were experienced by two subjects and were infectious eczematoid dermatitis, right leg edema, staphylococcal skin infection, and bilateral leg edema. None of the special interest adverse events led to study discontinuation.

This was a phase 2, single-arm, open-label study to evaluate the PK and safety of nemolizumab in adolescents with moderate to severe AD and severe pruritus. The PK results demonstrated in this study are consistent with previous data from studies of nemolizumab in adults with moderate to severe AD and severe pruritus. Nemolizumab 30 mg treatment in adolescents was associated with C max at 1-2 weeks after injection of the 60-mg loading dose, while steady state occurred at week 4 with C trough ranging from 2935 ± 1029 ng/mL to 3292 ± 2018 ng/mL over the treatment period up to week 16. Nemolizumab observed exposures in adolescents were comparable to those in adults receiving the same dosing regimens. The PK profile of nemolizumab in adolescents was described by a one-compartment model with linear elimination and first-order absorption with a lag time. The popPK analysis confirmed a similar PK profile in adults and adolescents and predicted a mean half-life of 16.7 ± 4.1 days. As for adults, the main intrinsic source of PK variability on exposure in adolescents was body weight, impacting both elimination (CL/F) and distribution (V/F), while albumin only slightly impacted CL/F. Incidence of ADA formation in the adolescent population was limited, and no ADA-positive sample had neutralizing antibodies.

The secondary objective of the study was to evaluate the efficacy of nemolizumab and to further characterize the relationship between nemolizumab systemic exposure and clinical efficacy endpoints (PK/PD relationship). Although this study had a small sample size and was open-label, efficacy data suggest that nemolizumab improved signs/symptoms of AD in adolescents to a degree comparable to adults. Silverberg et al. reported a reduction in EASI score of 68.5% at week 16 in adults treated in nemolizumab, which is quite similar to the 66.5% observed in this study [17] . PK/PD models developed in adults were able to describe nemolizumab individual efficacy profiles in adolescents for clinical endpoints, providing more evidence for similarity of exposure-response in adolescents and adults. AD is a heterogenous disease and defining clear biomarkers of responsiveness is critical towards elucidating and comparing the mechanism of action of specific therapies. Biomarker analysis in this study clearly identified a panel of ADrelated pro-inflammatory biomarkers (including CCL17, CCL20, CCL22, CCL27, VEGF, IL-1RA, and CCL18) that are upregulated in lesional skin (as compared to non-lesional skin) and are correspondingly downregulated in clinical responders (as defined by EASI75 and PP-NRS C 4) of nemolizumab. These biomarkers have been previously reported as clear indicators for disease severity and are likely major players in AD pathogenesis. A recent review on behalf of the International Eczema Council (IEC) indicated that data for CCL17 currently has the strongest evidence for correlation with AD severity, but the report also discusses the roles of CCL22 and CCL27 [18] . Notably, IEC suggested that CCL22 may be the best biomarker of disease response according to studies using different treatment approaches including crisaborole, cyclosporine, and fezakinumab [18, 19] . Interestingly, while CCL17 and CCL2 and CCL27 have been shown to attract type 2 cells to inflammatory sites [18, 19] , CCL27 has been described to induce the migration of skin-associated memory T cells into cutaneous sites [18] [19] [20] . While evaluating changes in biomarkers in subjects with moderate to severe AD before and after oral Janus kinase/SYK inhibition, Pavel et al. observed changes in CCL20 and CCL22, among other markers [21] . Additionally, decreases in CCL17 and CCL18 by dupilumab treatment were associated with clinical improvement [19] [20] [21] .

Study limitations include a small sample size, the lack of a placebo control, and the openlabel design.

Nemolizumab PK and safety profiles in adolescents with moderate to severe AD study are consistent with previous data from studies of nemolizumab in adults with moderate to severe AD. PK/PD models demonstrate similar exposure-response profiles in 12-to 17-year-old adolescents and adults for three clinical endpoints (EASI, IGA, and PP-NRS). Nemolizumab treatment reversed AD-related pro-inflammatory biomarkers in skin, indicating that the neuroimmune cytokine IL-31 is the central mediator of multiple pathways in AD.

Funding. This study and Rapid Service Fee were funded by Galderma R&D, Lausanne, Switzerland.

Authorship. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.

Author Contributions. All authors contributed to the study conception and design. Material preparation, data collection and analysis were performed by Dr Piketty, Mr Ahmad, Mr Loprete, Dr Krishnaswamy, and Dr Jabbar-Lopez. The first draft of the manuscript was written by Dr Piketty and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

Medical Writing and/or Editorial Assistance. The authors wish to thank Valerie Sanders, from Sanders Medical Writing, for providing editorial assistance.

Disclosures. Robert Sidbury has served as an investigator for Galderma, Regeneron, Pfizer, and UCB; Sady Alpizar has served as an investigator for Galderma; Vivian Laquer has served as an investigator for Galderma and her employer received research grants; Sunil Dhawan has served as an investigator for Galderma; William Abramovits has served as an investigator for Galderma; Luca Luprete, Faiz Ahmad, Zarif Jabbar-Lopez, Jayendar Krishnaswamy and Christophe Piketty are employees of Galderma. , 1996] ) and guidelines and in accordance with local requirements. Subjects and guardians were informed in the ICF that the results of this study may be included in publications.

Data Availability. The data that support the findings of this study are available from the corresponding author on reasonable request and with permission of the study's sponsor. The data are not publicly available due to reasons of sensitivity and other reasons.

Open Access. This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/bync/4.0/.

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