Table 1. Characteristics of the 25 Parenteral Cancer Therapies Included in the Analysis of Price Transparency.
Variable | No. of drugs (%) |
---|---|
Initial FDA approval year | |
2013-2017 | 10 (40.0) |
2008-2012 | 6 (24.0) |
Before 2008 | 9 (36.0) |
Molecule type | |
Small | 7 (28.0) |
Biologic | 17 (68.0) |
Other | 1 (4.0) |
Generic or biosimilar agent approveda | |
Yes | 9 (36.0) |
No | 16 (64.0) |
Orphan drug designationb | |
Yes | 20 (80.0) |
No | 5 (20.0) |
Breakthrough designationb | |
Yes | 11 (44.0) |
No | 14 (56.0) |
Oncologic disease areac | |
Hematologic | 11 (44.0) |
Pulmonary | 9 (36.0) |
Breast | 7 (28.0) |
Gastrointestinal | 7 (28.0) |
Hepatobiliary | 6 (24.0) |
Genitourinary | 5 (20.0) |
Cutaneous | 4 (16.0) |
Renal | 4 (16.0) |
Head/neck | 3 (12.0) |
Other | 3 (12.0) |
Gynecologic | 2 (8.0) |
2019 Medicare Part B spending (millions), $ | |
>500 | 7 (28.0) |
250-500 | 9 (36.0) |
<250 | 9 (36.0) |
Abbreviation: FDA, Food and Drug Administration.
Approval status as of April 26, 2021.
Includes designations for both original and supplemental FDA-approved indications.
Non–mutually exclusive categorizations.