Caregiver perspectives

Kateage 9,
living with
Rett syndrome,
with her caregivers

Kate’s Story with DAYBUE

  • Name: Kate M.

  • Age: 9 years old

  • Age at RTT diagnosis: 3.5 years old

  • Diagnosis: Classic Rett syndrome with genetic confirmation

  • Key symptoms: Speech and language regression, motor skill regression, repetitive hand behaviors, including mouthing

  • Comorbidities: Occasional constipation, treated with laxatives

  • Treatments: No daily medications to manage symptoms; attends occupational therapy to strengthen hand function, as well as speech and physical therapy

Kate’s parents, Jim and Jen, noticed meaningful improvements in Kate’s signs and symptoms of RTT, including:

  • Improved hand use
    Kate is able to use a spoon and point at and touch her tablet

  • Improved mood
    Her parents describe her as more peaceful—at home, at school, and in groups

  • Improved eye gaze
    Kate is better able to use her eye-gaze device to communicate with her family

Managing side effects

After starting DAYBUE, Kate began experiencing diarrhea. While it does not occur daily, when it occurs, it can happen several times a day and can require multiple diaper changes. Kate's parents worked with their healthcare team on management strategies for diarrhea.

  • In consultation with her healthcare team, Kate’s parents stopped giving her laxatives and instead started an antidiarrheal every day, which has helped make her bowel movements more solid

Important note

The experiences of Kate and her family may differ from those of other patients and families. Kate was a participant in the 12-week and open label extension trials with DAYBUE. Her experience on treatment is unique to her. Individual results may vary. Kate continues to take DAYBUE and is enrolled in Acadia Connect. Her family was compensated for participating in a photo shoot and sharing their story.

Request a representative for more information about the efficacy of DAYBUE.

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Important Safety Information and Indication

  • Warnings and Precautions

    • Diarrhea: In a 12-week study and in long-term studies, 85% of patients treated with DAYBUE experienced diarrhea. In those treated with DAYBUE, 49% either had persistent diarrhea or recurrence after resolution despite dose interruptions, reductions, or concomitant antidiarrheal therapy. Diarrhea severity was of mild or moderate severity in 96% of cases. In the 12-week study, antidiarrheal medication was used in 51% of patients treated with DAYBUE.

      Patients should stop taking laxatives before starting DAYBUE. If diarrhea occurs, patients should notify their healthcare provider, consider starting antidiarrheal treatment, and monitor hydration status and increase oral fluids, if needed. Interrupt, reduce dose, or discontinue DAYBUE if severe diarrhea occurs or if dehydration is suspected.

    • Weight Loss: In the 12-week study, 12% of patients treated with DAYBUE experienced weight loss of greater than 7% from baseline, compared to 4% of patients who received placebo. In long-term studies, 2.2% of patients discontinued treatment with DAYBUE due to weight loss. Monitor weight and interrupt, reduce dose, or discontinue DAYBUE if significant weight loss occurs.

  • Adverse Reactions: The common adverse reactions (≥5% for DAYBUE-treated patients and at least 2% greater than in placebo) reported in the 12-week study were diarrhea (82% vs 20%), vomiting (29% vs 12%), fever (9% vs 4%), seizure (9% vs 6%), anxiety (8% vs 1%), decreased appetite (8% vs 2%), fatigue (8% vs 2%), and nasopharyngitis (5% vs 1%).

  • Drug Interactions: Effect of DAYBUE on other Drugs

    • DAYBUE is a weak CYP3A4 inhibitor; therefore, plasma concentrations of CYP3A4 substrates may be increased if given concomitantly with DAYBUE. Closely monitor when DAYBUE is used in combination with orally administered CYP3A4 sensitive substrates for which a small change in substrate plasma concentration may lead to serious toxicities.

    • Plasma concentrations of OATP1B1 and OATP1B3 substrates may be increased if given concomitantly with DAYBUE. Avoid the concomitant use of DAYBUE with OATP1B1 and OATP1B3 substrates for which a small change in substrate plasma concentration may lead to serious toxicities.

  • Use in Specific Population: Renal Impairment

    • DAYBUE is not recommended for patients with moderate or severe renal impairment.

DAYBUE is available as an oral solution (200mg/mL).

  • Indication

DAYBUE is indicated for the treatment of Rett syndrome in adults and pediatric patients 2 years of age and older.

Please read the full Prescribing Information.

Important Safety Information and Indication

  • Warnings and Precautions

    • Diarrhea: In a 12-week study and in long-term studies, 85% of patients treated with DAYBUE experienced diarrhea. In those treated with DAYBUE, 49% either had persistent diarrhea or recurrence after resolution despite dose interruptions, reductions, or concomitant antidiarrheal therapy. Diarrhea severity was of mild or moderate severity in 96% of cases. In the 12-week study, antidiarrheal medication was used in 51% of patients treated with DAYBUE.

      Patients should stop taking laxatives before starting DAYBUE. If diarrhea occurs, patients should notify their healthcare provider, consider starting antidiarrheal treatment, and monitor hydration status and increase oral fluids, if needed. Interrupt, reduce dose, or discontinue DAYBUE if severe diarrhea occurs or if dehydration is suspected.

    • Weight Loss: In the 12-week study, 12% of patients treated with DAYBUE experienced weight loss of greater than 7% from baseline, compared to 4% of patients who received placebo. In long-term studies, 2.2% of patients discontinued treatment with DAYBUE due to weight loss. Monitor weight and interrupt, reduce dose, or discontinue DAYBUE if significant weight loss occurs.

  • Adverse Reactions: The common adverse reactions (≥5% for DAYBUE-treated patients and at least 2% greater than in placebo) reported in the 12-week study were diarrhea (82% vs 20%), vomiting (29% vs 12%), fever (9% vs 4%), seizure (9% vs 6%), anxiety (8% vs 1%), decreased appetite (8% vs 2%), fatigue (8% vs 2%), and nasopharyngitis (5% vs 1%).

  • Drug Interactions: Effect of DAYBUE on other Drugs

    • DAYBUE is a weak CYP3A4 inhibitor; therefore, plasma concentrations of CYP3A4 substrates may be increased if given concomitantly with DAYBUE. Closely monitor when DAYBUE is used in combination with orally administered CYP3A4 sensitive substrates for which a small change in substrate plasma concentration may lead to serious toxicities.

    • Plasma concentrations of OATP1B1 and OATP1B3 substrates may be increased if given concomitantly with DAYBUE. Avoid the concomitant use of DAYBUE with OATP1B1 and OATP1B3 substrates for which a small change in substrate plasma concentration may lead to serious toxicities.

  • Use in Specific Population: Renal Impairment

    • DAYBUE is not recommended for patients with moderate or severe renal impairment.

DAYBUE is available as an oral solution (200mg/mL).

  • Indication

DAYBUE is indicated for the treatment of Rett syndrome in adults and pediatric patients 2 years of age and older.

Please read the full Prescribing Information.