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Safety, Tolerability And Pharmacodynamics of DM-101PX in Birch Pollen Allergy (UPSIT)

30 de octubre de 2026 actualizado por: Desentum Oy

A Randomised, Double Blind, Placebo-controlled Study to Evaluate the Safety, Tolerability And Pharmacodynamics of Subcutaneous Immunotherapy With DM-101PX in Subjects With Birch Pollen Allergy

Randomized, double-blind placebo-controlled phase I trial with the primary aim to investigate safety and tolerability of DM-101-PX compared to placebo in birch pollen allergic adults. As an secondary objectives, the trial will also assess the number of participants receiving the maximum intended DM-101PX dose and to assess the effect of treatment with DM-101PX compared with placebo on blood allergy biomarkers. Expanded access to the study treatment is not available.

Descripción general del estudio

Estado

Reclutamiento

Descripción detallada

The study will be carried out in a single study site located in Germany.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

40

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

      • Hanover, Alemania, 30625
        • Reclutamiento
        • Fraunhofer Institute for Toxicology and Experimental Medicine ITEM
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 65 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Male or female, aged 18 to 65 years
  • Good general health
  • A documented clinical history of moderate to severe birch pollen-induced allergic rhinitis or rhinoconjunctivitis for at least 2 years with symptoms that interfere with daily activities or sleep
  • Bet v 1-specific IgE ≥0.7 kU/L (class 2) measured by ImmunoCAP® performed at the trial site at Screening or within 12 months prior to Screening
  • Positive SPT to Birch pollen whole allergen extract with a wheal diameter ≥3 mm (average of longest and orthogonal), with the negative control wheal diameter <2 mm and the positive (histamine) control wheal diameter ≥3 mm, performed at the trial site at Screening or within 12 months prior to Screening
  • Body weight ≥50 kg and body mass index within the range 18-35 kg/m2

Exclusion Criteria:

  • History or findings on physical examination of any significant disease or disorder which, in the opinion of the investigator, may put the individual at risk because of participation in the trial, influence the results of the trial or the participant's ability to participate in the trial
  • Significant rhinitis, sinusitis, and/or symptomatic respiratory allergy due to regular contact with allergens other than birch pollen that are expected to potentially interfere with the trial assessments, as assessed by the investigator
  • Persistent asthma that requires GINA Step 2 or higher treatment during the trial period, or required treatment within 4 weeks prior to Screening
  • History of uncontrolled asthma according to GINA classification in the 6 months prior to Screening or history of asthma deterioration that resulted in emergency treatment or hospitalization in the 12 months before Screening, or a life-threatening asthma attack (eg, one requiring intubation and mechanical ventilation) at any time in the past
  • Forced Expiratory Volume in one second (FEV1) <70 % of predicted, regardless of asthma status at Screening
  • History of severe drug allergy, severe angioedema, or systemic allergic reaction of Grade 3 or greater, according to the WAO classification (2024, see Section 12.5), due to any cause
  • History of acute hypersensitivity and/or anaphylaxis to protein therapeutics or components of formulation, including polyethylene glycol, or severe or significant allergies that in the opinion of the investigator could represent a substantial risk to the individual

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Triple

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: DM-101PX for cohort 1

Weekly subcutaneous administration of ascending doses of DM-101PX for 10 weeks with dose escalation starting from 0.2 µg with slightly varying injection volumes.

Subcutaneous injection of DM-101PX

Comparador de placebos: Placebo for cohort 1

Weekly subcutaneous administration of Placebo for 10 weeks

Placebo to match subcutaneous injection of DM-101PX

Experimental: Experimental: DM-101PX for cohort 2

Weekly subcutaneous administration of ascending doses of DM-101PX for 10 weeks with dose escalation starting from 0.2 µg with varying injection volumes

Subcutaneous injection of DM-101PX

Comparador de placebos: Placebo for cohort 2

Weekly subcutaneous administration of Placebo for 10 weeks

Placebo to match subcutaneous injection of DM-101PX

Experimental: Experimental: DM-101PX for cohort 3

Weekly subcutaneous administration of ascending doses of DM-101PX for 10 weeks with regimens consisting of 2 initial placebo s.c. injections, followed by 8 s.c. injections with escalating doses starting from 0.2 µg and with varying injection volumes.

Subcutaneous injection of DM-101PX

Comparador de placebos: Placebo for cohort 3

Weekly subcutaneous administration of Placebo for 10 weeks

Placebo to match subcutaneous injection of DM-101PX

Experimental: Experimental: DM-101PX for cohort 4

Weekly subcutaneous administration of ascending doses of DM-101PX for 10 weeks with regimens consisting of 2 initial placebo s.c. injections, followed by 8 s.c. injections with escalating doses starting from 0.2 µg and with constant varying injection volume.

Subcutaneous injection of DM-101PX

Comparador de placebos: Placebo for cohort 4

Weekly subcutaneous administration of Placebo for 10 weeks

Placebo to match subcutaneous injection of DM-101PX

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Treatment Emergent Adverse Events
Periodo de tiempo: From the first dose to until 3 months from the last dose

Occurrence of treatment emergent adverse events

From the first dose to until 3 months from the last dose
Adverse Events of Special Interest
Periodo de tiempo: From the first dose to until 3 months from the last dose

Occurrence of local injection site reactions and systemic allergic reactions

From the first dose to until 3 months from the last dose

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Subjects Reaching the Maximum Intended Dose
Periodo de tiempo: Through the treatment period, an average of 10 weeks

Number of subjects in each cohort who reach the maximum intended dose

Through the treatment period, an average of 10 weeks
Change in blood allergy biomarker levels
Periodo de tiempo: From baseline to 3 and 12 weeks, after completion of treatment

Change in the levels of Bet v 1-specific IgE, IgG1 and IgG4

From baseline to 3 and 12 weeks, after completion of treatment

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Philipp Badorrek, MD, Fraunhofer Institute for Toxicology and Experimental Medicine ITEM

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

29 de octubre de 2026

Finalización primaria (Estimado)

1 de marzo de 2027

Finalización del estudio (Estimado)

1 de mayo de 2027

Fechas de registro del estudio

Enviado por primera vez

20 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

20 de octubre de 2026

Publicado por primera vez (Actual)

27 de octubre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

3 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

30 de octubre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • DM-101-C-005

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan IPD

All individual participant data that underlie publicly available results will be considered for sharing

Marco de tiempo para compartir IPD

Anonymized participant data will be considered for sharing once the indication has been approved by a regulatory body, if there is legal authority to share the data and there is not a reasonable likelihood of participant reidentification.

Criterios de acceso compartido de IPD

Qualified researchers may request access to patient level data underlying the publication: patient level data will be anonymized and study documents will be redacted to protect the privacy of trial participants. Patient level data will be anonymized and study documents will be redacted to protect the privacy of trial participants after Desentum has received marketing authorization from major health authorities (e.g. FDA, EMA), has the legal authority to share the data, and has made the study results publicly available. Requests from qualified researchers will be reviewed by the Sponsor, and data will be shared only for scientifically sound research purposes, subject to a signed data sharing agreement and in compliance with applicable data protection legislation and participant consent.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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