Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

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

1 giugno 2026 aggiornato da: 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.

Panoramica dello studio

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Stimato)

50

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • California
      • San Francisco, California, Stati Uniti, 94143
        • University of California, San Francisco
        • Investigatore principale:
          • Sabine Mueller, MD, PhD, MAS
        • Contatto:
          • PNOC Operations Office
          • Numero di telefono: 877-827-3222
          • Email: PNOC039@ucsf.edu

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto

Accetta volontari sani

No

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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
Altri nomi:
  • Accutan
Perform blood draw
Altri nomi:
  • Prelievo di campioni di sangue
Undergo photography
Participants will be asked to complete questionnaires
Altri nomi:
  • Health-Related Quality of Life Questionnaires
Perform stool sample collection
Altri nomi:
  • Stool Sample collection
Sperimentale: 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
Altri nomi:
  • Prelievo di campioni di sangue
Undergo photography
Participants will be asked to complete questionnaires
Altri nomi:
  • Health-Related Quality of Life Questionnaires
Perform stool sample collection
Altri nomi:
  • Stool Sample collection
Given Orally
Altri nomi:
  • Vibramicina
  • Doryx

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Proportion of Participants who experienced acneiform rash
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Sabine Mueller, MD, PhD, MAS, University of California, San Francisco

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

30 agosto 2026

Completamento primario (Stimato)

30 agosto 2029

Completamento dello studio (Stimato)

30 marzo 2030

Date di iscrizione allo studio

Primo inviato

1 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

1 giugno 2026

Primo Inserito (Effettivo)

5 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

5 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

1 giugno 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

Descrizione del piano IPD

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

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO
  • LINFA

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Isotretinoin

Sottoscrivi