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. Author manuscript; available in PMC: 2020 Aug 3.
Published in final edited form as: Gynecol Oncol. 2019 Jun 4;154(2):294–301. doi: 10.1016/j.ygyno.2019.04.001

Table 3:

IPA-Related Treatment-Emergent Adverse Events with CTCAE Grade ≥3 by System Organ Class

Cohort 1 Cohort 2 Cohort 3 Cohort 4 Cohort 5 Expansion Cohort Overall
N=37
n (%)
Dose of Ipafricept (Q3W)
System Organ Class/
5 mg/kg
N=3
n (%)
10 mg/kg
N=4
n (%)
2 mg/kg
N=8
n (%)
4 mg/kg
N=9
n (%)
6 mg/kg
N=6
n (%)
6 mg/kg
N=7
n (%)
Patients reporting ≥1 IPA related TEAE with CTCAE≥ Grade 3 3 (100.0) 0 1(12.5) 0 1(16.7) 3(42.9) 8(21.6)
Investigations 3 (100) 0 0 0 0 3(42.9) 6(16.2)
 Neutropenia 3 (100) 0 0 0 0 3(42.9) 5(13.5)
Metabolism and nutrition disorders 0 0 1(12.5) 0 0 0 1(2.7)
 Hypophosphatemia 0 0 1(12.5) 0 0 0 1(2.7)
Gastrointestinal disorders 0 0 0 0 1 (16.7) 0 1(2.7)
 Diarrhea 0 0 0 0 1 (16.7) 0 1(2.7)
Nervous system disorders 0 0 0 0 0 1(14.3) 1(2.7)
 Neuropathy peripheral 0 0 0 0 0 1(14.3) 1(2.7)