PaTHway Phase 3 Trial Analysis
Key Secondary Endpoints:
Patient Reported Symptom & Quality of Life Domains
60
50
40
HPES Symptom
Physical domain
score
30
20
10
0
HH
HH
Weeks
p-value = 0.0038
50
40
HPES Symptom
Cognitive domain
score
30
20
10
26
0
Weeks
КЯНН
p-value = 0.0055
50
26
40
40
HPES Impact
Physical Functioning
domain score
30
20
20
HH
HOH
10
10
0
Weeks
p-value = 0.0046
TransCon PTH
50
50
26
HPES Impact
Daily Life domain
score
40
40
HH
30
30
HH
20
20
10
10
0
Weeks
Placebo
p-value = 0.0061
55
PaTHway
TRIAL
SF-36
Physical Functioning
subscale score
50
45
45
40
40
35
26
26
Weeks
All prespecified key secondary endpoints demonstrated statistically
significant improvement compared to control
P-values are TransCon PTH vs Control.
For HPES, lower scores indicate improvement; for SF-36, higher scores indicate
improvement.
20
Data on file, Ascendis Pharma 2022.
TransCon PTH is an investigational product candidate.
For investor communication only.
Not for use in product promotion. Not for further distribution.
p-value = 0.0347
26
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