People with pulmonary arterial hypertension (PAH) who took a once-daily investigational inhaled treatment called treprostinil palmitil inhalation powder (TPIP) maintained gains in walking distance and other health measures through 12 months, according to an ongoing study.
Although TPIP is not approved by the U.S. Food and Drug Administration (FDA), these findings are encouraging as a phase 3 trial is underway to further study its safety and effectiveness.
TPIP is a once-daily dry-powder form of treprostinil palmitil for PAH. After it’s inhaled, treprostinil palmitil is converted into treprostinil in the lungs, where it relaxes blood vessels and helps lower pressure in the pulmonary arteries.
PAH treatments can come in several forms, including oral, inhaled, subcutaneous, and intravenous options.
The 12-month update came from a 24-month extension study that enrolled 91 people at 45 sites globally who had completed earlier TPIP studies. Some had already been taking TPIP, while others crossed over from a placebo (inactive treatment) to TPIP in the extension.
By month 12, researchers found that:
As with all treatments, TPIP may cause side effects. Researchers found that TPIP was generally well tolerated, with no newly identified safety concerns through month 12. The most common side effects included:
Because there was no placebo comparison during the extension, the study can’t show cause and effect as clearly as a randomized, blinded trial.
A larger study to confirm these findings is already underway. The phase 3 PALM-PAH trial is testing once-daily TPIP against placebo in adults with PAH.
On myPHteam, people share their experiences with pulmonary hypertension, get advice, and find support from others who understand.
If a once-daily inhaled PAH treatment became available, what would matter most to you — symptom relief, convenience, side effects, or something else? Let others know in the comments below.
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