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Adult Patients Starting UPTRAVI

Setting PAH treatment goals and expectations

When you decide to start your adult patient on treatment with UPTRAVI, it’s important to set goals and expectations with them.

Before starting UPTRAVI, remind your adult patient of the following:

  • Anticipate a call from your specialty pharmacy to alert you of your next shipment of UPTRAVI
  • Do not change your dose or stop taking UPTRAVI unless your doctor tells you to do so1
  • Understand expectations for potential side effects. Follow up with your doctor if you have side effects that you cannot tolerate1
  • Try to take UPTRAVI with food. This may help you tolerate the dose better if you are having side effects with UPTRAVI1
  • After the dose adjustment phase, you will have found your personal maintenance dose of UPTRAVI. This will be the dose you continue to take on a regular basis, unless your doctor tells you otherwise1

UPTRAVI Dose Adjustment Phase helps meet individual adult patient needs1

Your adult patient's recommended starting dose is 200 mcg twice daily. UPTRAVI dosing is unique to each patient based on how their body responds and adjusts to treatment. The dose adjustment phase is how you find your patient's personal maintenance dose.

Titrating UPTRAVI doses graphic Titrating UPTRAVI doses mobile graphic
Tablet not shown at actual size. Tolerability may be improved when taken with food.

*Once daily for adult patients with moderate hepatic impairment (Child-Pugh class B) and co-administration with moderate CYP2C8 inhibitors (eg, clopidogrel, deferasirox, and teriflunomide). Increase in increments of 200 mcg once daily at weekly intervals.

  • If a dose of UPTRAVI is missed, patients should take the missed dose as soon as possible unless the next dose is within the next 6 hours
  • If treatment is missed for 3 days or more, restart UPTRAVI at a lower dose and then retitrate
Titrating UPTRAVI doses mobile graphic
Actor portrayal

After the dose adjustment phase1

Once each patient reaches their personal dose (maintenance), a single-tablet equivalent is prescribed BID. For adult patients, there are 8 different single-tablet strengths of UPTRAVI, each a unique color.

UPTRAVI offers a range of dose strengths to accommodate each adult patient’s personal maintenance dose

pill-2
200 mcg Light yellow
pill-4
400 mcg Red
pill-6
600 mcg Light violet
pill-8
800 mcg Green
pill-10
1000 mcg Orange
pill-12
1200 mcg Dark violet
pill-14
1400 mcg Dark yellow
pill-16
1600 mcg Brown
Comparison of pill and dime
Size shown in relation to a dime for proportional comparison. Tablet not shown at actual size. Actual tablet size is 7 mm.

Alternate methods of administration for patients who cannot swallow tablets whole1

Apple or orange juice

Apple or orange juice icon

UPTRAVI 100 mcg or 150 mcg film-coated tablets can be dispersed and administered in apple or orange juice. Do not disperse the tablet(s) in water or milk.

  • Do not crush or split the tablet(s)
  • At least 1 mL of juice per tablet is recommended
  • Add the juice to the required number of tablet(s) per dosing schedule
  • Wait for 5 minutes and then stir until the tablets are dispersed
  • Administer the mixture immediately after dispersion
  • Do not store tablets that are mixed with juice for later use

Soft foods

Soft foods icon

Alternatively, UPTRAVI 100 mcg and 150 mcg tablets can also be administered with soft foods such as yogurt, applesauce, or mashed banana.

  • Cover the required number of tablets with soft food.
  • Administer the mixture immediately
  • To ensure no tablet residue is left, add more soft food and administer the contents immediately
  • Do not store tablets that are mixed with soft food for later use

UPTRAVI Offers Oral Administration With Similar Efficacy at Every Dose Group in Adults1

Time to first disease progression event in GRIPHON by dose group3

Percent of patients without an event across UPTRAVI low-dose, medium-dose, high-dose, and placebo groups desktop curve Percent of patients without an event across UPTRAVI low-dose, medium-dose, high-dose, and placebo groups mobile curve

Efficacy by dose group of UPTRAVI vs placebo3†:

  • 40% RISK 
    REDUCTION
    (low dose: 200 mcg to 400 mcg)
    HR 0.60 (95% CI: 0.41, 0.88)
  • 47% RISK 
    REDUCTION
    (medium dose: 600 mcg to 1000 mcg)
    HR 0.53 (95% CI: 0.38, 0.72)
  • 36% RISK 
    REDUCTION
    (high dose: 1200 mcg to 1600 mcg)
    HR 0.64 (95% CI: 0.49, 0.82)

UPTRAVI doses were achieved across the 3 prespecified groups in the GRIPHON trial

  • 200 mcg to 400 mcg BID (low dose): 23% of patients (n=133)
  • 600 mcg to 1000 mcg BID (medium dose): 31% of patients (n=179)
  • 1200 mcg to 1600 mcg BID (high dose): 43%
     of patients (n=246)
Oral Administration Twice-daily dosing1
No needles, pumps, or inhalers

Not adjusted for multiplicity.

In the UPTRAVI group, 14 patients discontinued the 200 mcg twice-daily dosage during the dose adjustment phase and 1 patient received doses different from the per protocol dosing; all 15 were assigned to 0imcg and are not reported here.

§UPTRAVI IV is available for patients who are temporarily unable to take oral therapy.

BID=twice daily; CI=confidence interval; GRIPHON=Prostacyclin (PGI2) Receptor Agonist In Pulmonary Arterial HypertensION; HR=hazard ratio; IV=intravenous.

References: 1. UPTRAVI (selexipag) full Prescribing Information. Actelion Pharmaceuticals US, Inc. 2. McLaughlin V, Farber HW, Highland KB, et al. Disease characteristics, treatments, and outcomes of patients with pulmonary arterial hypertension treated with UPTRAVI in real-world settings from the SPHERE registry (SelexiPag: tHe usErs dRug rEgistry). J Heart Lung Transplant. 2024;43(2):272-283. 3. Kingman M, Archer‍-‍Chicko C, Bartlett M, et al. Management of prostacyclin side effects in adult patients with pulmonary arterial hypertension. Pulm Circ. 2017‍;‍7‍(‍3‍)‍:‍598‍-‍608.