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Opening doors to help your patients with APDS move forward

Enrolling your patients

in APDS Assist is quick and simple to do

1
Complete the enrollment form
2
Have your patient fill out and sign the consent form to receive
APDS Assist Support Services
3
Fax the enrollment form, the patient consent form, and any
additional documentation to APDS Assist at 1-833-850-2727
download enrollment form
Connect with a

Care Coordinator at APDS Assist

If you or your office a needs to get in contact with a Care Coordinator,
call 1-866-796-APDS (2737) from 8 AM-8 PM ET, Monday-Friday.

A Care Coordinator can also connect you
to a pharmacist.

Starter Program

Our commitment is to get your patient started on Joenja as quickly as possible while we work with your office to
process any insurance requirements.

Patient support

ACEs* can help your patients connect with local and nationwide support
groups and educational resources
along their Joenja journey.

Helping with coverage

Access to Joenja is a priority of
APDS Assist. Depending on the patient’s insurance and other eligibility criteria,
a Care Coordinator can help
identify financial resources.
*Please note that ACEs do not offer medical or treatment advice or replace discussions with a physician.
Learn about the

APDS Assist team

Watch these informative videos to enhance the conversations you may be having with patients about APDS Assist.

Indications and Usage

JOENJA® (leniolisib) is a kinase inhibitor indicated for the treatment of activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS) in adult and pediatric patients 12 years of age and older.

Important Safety Information

Verify pregnancy status in females of reproductive potential prior to initiating treatment with JOENJA.

Indications and Usage

JOENJA® (leniolisib) is a kinase inhibitor indicated for the treatment of activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS) in adult and pediatric patients 12 years of age and older.

Important Safety Information

Verify pregnancy status in females of reproductive potential prior to initiating treatment with JOENJA.

JOENJA may cause fetal harm when administered to a pregnant woman. Advise patients of the potential risk to a fetus and to use highly effective methods of contraception during treatment with JOENJA and for 1 week after the last dose of JOENJA.

Live, attenuated vaccinations may be less effective if administered during JOENJA treatment.

Use of JOENJA in patients with moderate to severe hepatic impairment is not recommended. There is no recommended dosage for patients weighing less than 45 kg.

The most common adverse reactions (incidence >10%) seen in clinical trials were headache, sinusitis, and atopic dermatitis.

Seven (33%) patients receiving JOENJA developed an absolute neutrophil count (ANC) between 500 and 1500 cells/microL. No patients developed an ANC <500 cells/ microL and there were no reports of infection associated with neutropenia.

Before prescribing JOENJA, please read the full Prescribing Information.