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MOST COMMON ADVERSE EVENTS

JASCAYD® had a favorable tolerability and safety profile1

JASCAYD® treatment does not require liver or lab monitoring2

ADVERSE EVENTS IN ≥10% OF JASCAYD® PATIENTS AND MORE OFTEN THAN PLACEBO1

 

Placebo +/- background AF
(n=393)

JASCAYD® 18 mg +/-
background nintedanib (n=392)

Diarrhea

18%

42%

Upper respiratory tract infection

11%

14%

Weight decreased

10%

12%

Decreased appetite

7%

10%

Nausea

7%

9%

Fatigue

6%

8%

Headache

6%

7%

Back pain

4%

7%

Vomiting

5%

6%

Respiratory tract infection

3%

6%

ADVERSE EVENTS IN ≥10% OF JASCAYD® PATIENTS AND MORE OFTEN THAN PLACEBO1

 

Placebo +/- background AF (n=393)

JASCAYD® 9 mg +/- background nintedanib (n=392)

Diarrhea

18%

32%

Upper respiratory tract infection

11%

12%

Weight decreased

10%

11%

Decreased appetite

7%

10%

Nausea

7%

9%

Fatigue

6%

8%

Headache

6%

6%

Back pain

4%

6%

Vomiting

5%

5%

Respiratory tract infection

3%

4%

DIARRHEA

Frequency of diarrhea varied across treatment groups in the trial2

The most frequent adverse event associated with JASCAYD® 18 mg was diarrhea, and in most cases it was mild to moderate in intensity and generally occurred within the first 3 months of treatment2

DIARRHEA
DIARRHEA

Only 1% of patients taking JASCAYD® 18 mg monotherapy discontinued treatment due to diarrhea events3

OTHER SAFETY AND TOLERABILITY CONSIDERATIONS

Safety and tolerability considerations when prescribing JASCAYD®2

Safety and tolerability considerations report
Diarrhea, nausea, and decreased appetite were frequently reported adverse reactions, particularly with concomitant use of nintedanib or pirfenidone.
Safety and tolerability considerations dose
Treatment may also be associated with dose-dependent weight loss, particularly with concomitant use of nintedanib.

Psychological disorders are common in PPF and IPF. While no imbalance was seen with JASCAYD® vs placebo in psychiatric events, routine monitoring is recommended2

References

  1. Data on file. Boehringer Ingelheim International GmbH. FIBRONEER-IPF CTR. 2025.

  2. JASCAYD® UAE Local SmPC; May 2026.

  3. Oldham JM, Azuma A, Kreuter M, et al. Nerandomilast in idiopathic pulmonary fibrosis: data from the whole follow-up period of the FIBRONEER-IPF trial. Am J Respir Crit Care Med. Published online February 21, 2026.

  4. Oldham JM, Azuma A, Kreuter M, et al. Effect of nerandomilast on clinical outcomes in patients with idiopathic pulmonary fibrosis (IPF): data from final database lock of the FIBRONEER-IPF trial. Presented at: European Respiratory Society (ERS) International Congress; September 2025; Vienna, Austria. Poster available from: https://www.globalmedcomms.com/respiratory/ERS2025/Oldham1

MLR ID: PC-AE-102892
Expiry Date: 10/05/2028

Vault id: WP-AE-100020