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In this open-label study, Joenja results were compared to each child’s baseline measurements.

  • Lymph node size was measured for each person before and after treatment with Joenja to compare the reduction in size
  • The results showed that the average size of lymph nodes decreased in children taking Joenja

This chart shows changes in lymph node size for 19 patients. On average, the lymph nodes got smaller. The shorter thin line in the middle of the orange bar shows the average. The longer thin line in the middle of the orange bar shows that results varied from person to person.


  • Children in the clinical trial had their naïve B cells measured at 12 weeks
  • A naïve B cell is a type of immune cell that has never been exposed to a foreign substance, such as a virus, bacteria, or other invaders
  • The results showed an increase in naïve B cells with Joenja. An increase in naïve B cells can help the body fight infections

The colored bar shows the average rise in naïve B cells after treatment. Because the bar goes up, it means patients generally had more naïve B cells. The thin line shows how much this varied from person to person.

  • The spleen plays an important role in filtering out infections from our blood. When the spleen becomes enlarged, it may not function properly
  • Reduction in spleen size was consistent across all age groups

The orange bar shows the decrease in spleen size for the 21 patients in the study, and the vertical line shows the different results each patient saw in their spleen size. Some patients saw a bigger reduction in their spleen size compared to others.

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Important Safety Information

Tell your healthcare provider if you are pregnant or plan to become pregnant. JOENJA may harm your unborn baby. Your healthcare provider will do a pregnancy test before you start receiving JOENJA.

Important Safety Information

Tell your healthcare provider if you are pregnant or plan to become pregnant. JOENJA may harm your unborn baby. Your healthcare provider will do a pregnancy test before you start receiving JOENJA.

Use effective birth control to prevent pregnancy while taking JOENJA and for one week after you stop taking JOENJA. If you plan to become pregnant, continue taking your birth control for one week after stopping JOENJA. Talk to your doctor about what type of birth control method is right for you while taking JOENJA.

It is not known if JOENJA passes into your breast milk. Talk to your doctor about the best way to feed your baby if you take JOENJA.

Tell your healthcare provider and pharmacist about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. JOENJA and certain other medicines may affect each other.

Tell your healthcare provider if you are scheduled to receive an immunization (vaccine). JOENJA may affect how well a vaccine works.

Discontinue JOENJA and seek immediate medical attention if you develop any signs and symptoms of serious allergic reactions including itching, skin redness, hives, rash, difficulty breathing, or swallowing.

The most common side effects of JOENJA in adults and pediatric patients 12 years of age and older include headache, inflammation of sinuses, weight gain, and dry, itchy, and inflamed skin (eczema).

The most common side effects of JOENJA in pediatric patients 4 to 11 years of age include headache, cough, pyrexia, vomiting, diarrhea, and sinusitis.

These are not all the possible side effects of JOENJA. Tell your healthcare provider about any side effect that bothers you or does not go away. You can also
report negative side effects to FDA at 1-800-FDA-1088 or www.fda.gov/medwatch, or Pharming Medical Affairs at (800) 930-5221.

For more information, please see the full Prescribing Information.

Joenja is available in 40 mg, 50 mg, and 70 mg tablets.

Approved Use

JOENJA® (leniolisib) is a prescription medicine that is used to treat activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS) in adults and children 4 years of age and older.

INFORMACION DE SEGURIDAD IMPORTANTE

Informe a su proveedor de atención médica si está embarazada o planea quedar embarazada. JOENJA puede dañar al bebé en gestación. Su proveedor de atención médica le hará una prueba para la detección del embarazo antes de que empiece a recibir JOENJA.

INFORMACION DE SEGURIDAD IMPORTANTE

Utilice un método anticonceptivo eficaz para evitar el embarazo mientras toma JOENJA y durante una semana después de dejar de tomarlo. Si planea quedar embarazada, siga tomando su método anticonceptivo durante una semana después de dejar de tomar JOENJA. Hable con su médico sobre el tipo de método anticonceptivo adecuado para usted mientras toma JOENJA.

Se desconoce si JOENJA pasa a la leche materna. Hable con su médico sobre la mejor manera de alimentar a su bebé si toma JOENJA.

Informe a su proveedor de atención médica y farmacéutico todos los medicamentos que toma, incluidos los medicamentos de venta con receta y de venta libre, las vitaminas y los suplementos a base de hierbas. JOENJA y ciertos medicamentos pueden afectarse entre sí.

Informe a su proveedor de atención médica si tiene programado recibir una inmunización (vacuna). JOENJA puede afectar la eficacia de una vacuna.

Interrumpa JOENJA y busque atención médica inmediata si presenta algún signo y síntoma de reacciones alérgicas graves, incluidos picazón, enrojecimiento de la piel, urticaria, erupción, dificultad para respirar o para tragar.

Los efectos secundarios más frecuentes de JOENJA incluyen dolor de cabeza; inflamación de los senos paranasales; aumento de peso; y sequedad, picazón e inflamación de la piel (eccema). Estos no son todos los posibles efectos secundarios de JOENJA. Informe a su proveedor de atención médica sobre cualquier efecto secundario que le cause molestias o que no desaparezca.

También puede informar efectos secundarios negativos a la Administración de Alimentos y Medicamentos (Food and Drug Administration, FDA) al 1-800-FDA-1088 o visitar www.fda.gov/medwatch, o a asuntos médicos de Pharming al (800) 930-5221.

USO APROBADO

JOENJA® (leniolisib) es un medicamento de venta con receta que se utiliza para tratar el síndrome de fosfoinositida 3-cinasa delta (PI3Kδ) activada (APDS) en adultos y niños de 12 años o más.

Para obtener más información, consulte la Información de prescripción completa.