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Isotretinoin vs. Doxycycline for Acneiform Rash in Patients Receiving Drugs That Target the MAPK Pathway (PNOC039)

2026年6月1日 更新者:University of California, San Francisco

A Phase 2 Study of Isotretinoin vs. Doxycycline for Acneiform Rash in Patients Receiving Drugs That Target the MAPK Pathway

A phase 2 study testing the efficacy of isotretinoin versus doxycycline in treating participants who develop a acneiform rash caused by standard of care, tumor-directed therapies targeting the mitogenactivated protein kinase (MAPK) pathway.

調査の概要

詳細な説明

PRIMARY OBJECTIVES:

1. To compare the efficacy of the isotretinoin and doxycycline after 12 weeks of therapy in patients who develop an acneiform rash caused by a MAPK pathway-inhibitor, measured by the NCI Common Terminology Criteria for Adverse Events (CTCAE) v5.0.

EXPLORATORY OBJECTIVES:

  1. To assess feasibility of a centralized dermatology review to confirm rash grading and response to treatment.
  2. The participants' Multinational Association of Supportive Care in Cancer (MASCC) Epidermal Growth Factor Receptor Inhibitors (EGFRI) Skin Toxicity Tool (MESST) scores will be compared to CTCAE grading.
  3. To measure time to rash response by comparing CTCAE rash grading.
  4. To measure the change in quality-of-life scores from baseline to after 12 weeks of doxycycline or isotretinoin therapy using the Children's Dermatology Life Quality Index (CDLQI) and Dermatology Life Quality Index (DLQI).
  5. To record adverse events caused by doxycycline or isotretinoin and any cutaneous adverse events thought to be caused by the targeted agent per CTCAE v5.0.
  6. To characterize cutaneous toxicities across participants with different skin colors and tones.
  7. To measure the frequency of dose alterations in the MAPK inhibitor and then compare between the two study arms.
  8. To evaluate the number of participants who require retreatment for a rash 3 months after stopping study treatment.
  9. To describe the microbiome profile in participants receiving doxycycline and isotretinoin.

OUTLINE:

Participants will be randomized to receive 12 weeks of isotretinoin or doxycycline. Participants are followed at the end of treatment, day 30, 3 months and 6 months after treatment.

研究の種類

介入

入学 (推定)

50

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Jannerfer An
  • 電話番号:877-827-3222
  • メール:PNOC039@ucsf.edu

研究場所

    • California
      • San Francisco、California、アメリカ、94143
        • University of California, San Francisco
        • 主任研究者:
          • Sabine Mueller, MD, PhD, MAS
        • コンタクト:
          • PNOC Operations Office
          • 電話番号:877-827-3222
          • メール:PNOC039@ucsf.edu

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子
  • 大人

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. Participants must have developed either a grade 2, 3, or 4 rash categorized as acneiform while taking tumor-directed therapy that targets the MAPK pathway.

    • Acneiform rash will be defined according to CTCAE v5.0 as a disorder characterized by an eruption of papules and pustules, typically appearing in face, scalp, upper chest and back.

      1. Grade 2 = Papules and/or pustules covering 10-30% body surface area (BSA), which may or may not be associated with symptoms or of pruritus or tenderness; associated with psychosocial impact; limiting instrumental Activities of Daily Living (ADL); papules and/or pustules covering > 30% BSA with or without mild symptoms.
      2. Grade 3 = Papules and/or pustules covering > 30% BSA with moderate or severe symptoms; limiting self-care ADL; associated with local superinfection with oral antibiotics indicated.
      3. Grade 4 = Life-threatening consequences; papules and/or pustules covering any % BSA, which may or may not be associated with symptoms of pruritus or tenderness and are associated with extensive superinfection with IV antibiotics indicated.
  2. Prior Therapy: Participants may have received either doxycycline or isotretinoin in the past for treatment of their targeted therapy induced rash or acne. However, if they took doxycycline or another tetracycline antibiotic for a rash caused by a targeted therapy or for acne, the last dose must have been at least 4 weeks before study registration. If a participant took isotretinoin for any reason, the last dose must be at least 6 months prior to study registration.
  3. Age. 12-39 years old.
  4. Organ Function Requirements.

    a. Adequate Liver Function Defined as:

    • Total bilirubin ≤ 1.5 x upper limit of normal (ULN) for age; in presence of Gilbert's syndrome, total bilirubin < 3 x ULN or direct bilirubin < 1.5 x ULN
    • alanine aminotransferase (ALT) ≤ 3 x ULN
    • aspartate aminotransferase (AST) ≤ 3 x ULN.
    • Serum triglycerides < 500 mg/dL or < 5.7 mmol/L
  5. Due to the harmful effects of isotretinoin and doxycycline on the developing human fetus women of child-bearing potential and men must agree to use adequate contraception (as recommended by the iPLEDGE system if residing in the United States for those who will take isotretinoin) prior to study entry, for the duration of study participation, and one (1) month after completion of isotretinoin and doxycycline administration. If a participant requires contraception, they will require two forms of contraception as outlined by the iPLEDGE system. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately. The proper steps in the iPLEDGE system must also be taken.
  6. Participants must be able and willing to take a gelatin capsule.
  7. Participants must be able to swallow pills.
  8. A legal parent/guardian or participant must be able to understand, and willing to sign, a written informed consent and assent document, as appropriate.

Exclusion Criteria:

  1. History of allergic reactions attributed to compounds of similar chemical or biologic composition to doxycycline or isotretinoin, or other agents used in study. Participants also must not have a paraben allergy.
  2. Participants taking any medications listed must be discussed with study chair(s).
  3. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, other than skin infection in setting of rash.
  4. Women of childbearing potential must not be pregnant or breast-feeding.
  5. Participants who report active suicidal ideation due to isotretinoin's black box warning.
  6. Participants who refuse to be photographed for the centralized dermatology review.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Arm A: Isotretinoin

Participants randomized to the isotretinoin arm will be enrolled in the iPLEDGE program prior to treatment initiation. Female participants of childbearing potential will undergo a urine or serum pregnancy test as required for iPLEDGE registration. Participants will receive oral isotretinoin daily at a dose based on body weight, ranging from 10 mg to 40 mg, for up to 12 weeks. Treatment will consist of three consecutive 28-day cycles.

Participants will undergo follow-up at the end of treatment and at 30 days, 3 months, and 6 months after treatment completion for safety monitoring and post-treatment assessments, until withdrawal from the study or death, whichever occurs first.

Given Orally
他の名前:
  • アキュテイン
Perform blood draw
他の名前:
  • 採血
Undergo photography
Participants will be asked to complete questionnaires
他の名前:
  • Health-Related Quality of Life Questionnaires
Perform stool sample collection
他の名前:
  • Stool Sample collection
実験的:Arm B: Doxycycline
Participants randomized to the doxycycline arm will receive oral doxycycline daily at a body weight-based dose of 50 mg or 100 mg for up to 12 weeks. Treatment will consist of three consecutive 28-day cycles. Participants will undergo follow-up at the end of treatment and at 30 days, 3 months, and 6 months after treatment completion for safety monitoring and post-treatment assessments, until withdrawal from the study or death, whichever occurs first.
Perform blood draw
他の名前:
  • 採血
Undergo photography
Participants will be asked to complete questionnaires
他の名前:
  • Health-Related Quality of Life Questionnaires
Perform stool sample collection
他の名前:
  • Stool Sample collection
Given Orally
他の名前:
  • ビブラマイシン
  • ドリックス

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Proportion of Participants who experienced acneiform rash
時間枠:Up to 12 weeks following treatment
The proportion of participants who experience a Grade < 2 acneiform rash at week 12 while receiving non-investigational treatment for cancer that targets the mitogen activated protein kinase (MAPK) pathway as classified by the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE version 5.0) and 95% confidence interval will be reported.
Up to 12 weeks following treatment

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Sabine Mueller, MD, PhD, MAS、University of California, San Francisco

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年8月30日

一次修了 (推定)

2029年8月30日

研究の完了 (推定)

2030年3月30日

試験登録日

最初に提出

2026年6月1日

QC基準を満たした最初の提出物

2026年6月1日

最初の投稿 (実際)

2026年6月5日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月5日

QC基準を満たした最後の更新が送信されました

2026年6月1日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

De-identified datasets may be shared with research collaborators during the course of the study.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

はい

米国FDA規制機器製品の研究

いいえ

米国で製造され、米国から輸出された製品。

はい

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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