Doptelet
Doptelet has an established safety profile1,2
Adverse reactions with a frequency ≥10% in adults with chronic ITP treated with Doptelet—
pooled data from clinical trials.1*
Adverse Reaction | Doptelet (N=128) % | Placebo (N=22) % |
---|---|---|
Headache | 31 | 14 |
Fatigue | 28 | 9 |
Contusion | 26 | 18 |
Epistaxis | 19 | 18 |
Upper Respiratory Tract Infection | 15 | 5 |
Arthralgia | 13 | 0 |
Gingival Bleeding | 13 | 0 |
Petechiae | 11 | 9 |
Nasopharyngitis | 10 | 0 |
Doptelet has no reported interactions with statins, no cataracts precautions, and no associated liver damage.1,3†
*The American Society of Hematology (ASH) guidelines define a durable response as platelet count ≥30x109/L and at least doubling of the baseline count at 6 months.4
†Doptelet had no significant liver damage reported in clinical trials. Therefore, no additional liver function monitoring is required.2
Doptelet Safety and Tolerability
Thrombotic/Thromboembolic Complications1
In clinical trials in patients with chronic ITP, 7% (9/128) of patients treated with Doptelet developed a thromboembolic event
Serious Adverse Reactions1,2
Serious adverse reactions that occurred more frequently in patients with chronic ITP treated with Doptelet (9%; 12/128) compared to placebo (5%; 1/22) included headache, occurring in 1.6% (2/128)
Adverse reactions resulting in discontinuation of Doptelet that were reported in more than 1 patient included headache, occurring in 1.6% (2/128)
- DOPTELET (avatrombopag) [prescribing information]. Durham, NC: AkaRx, Inc; 2021.
- Jurczak W, Chojnowski K, Mayer J, et al. Phase 3 randomised study of avatrombopag, a novel thrombopoietin receptor agonist for the treatment of chronic immune thrombocytopenia. Br J Haematol. 2018;183(3):479-490.
- DOPTELET (avatrombopag) [patient information leaflet]. Durham, NC: AkaRx, Inc; 2021.
- Neunert C, Terrell DR, Arnold DM, et al. American Society of Hematology 2019 guidelines for immune thrombocytopenia. Blood Adv. 2019;3(23):3829-3866.