A Detailed Analysis of the Past 20 Years of US FDA-Approved Prescription to Over-the-Counter Switches
Objectives This evaluation assesses the quantity, uniqueness, and innovative nature of the past 20 years of Rx-to-OTC (RTO) switches, where a current prescription (Rx) product is reclassified for over-the-counter (OTC) status. Broadening access to more OTC drugs with well-established safety and efficacy could help to reduce healthcare expenditure and address public health challenges. Methods The FDA-maintained RTO switch list website was accessed to generate the primary dataset. Each product listed was assessed for the current OTC availability in the United States of its active ingredient, pharmacological class, and indication to determine its innovative quality. Descriptive statistics were employed in this study. Results From January 2002 through August 2022 there were 45 RTO switches. Among these, 51.1% involved a new to OTC active ingredient, 22.2% involved a new pharmacological class, 6.6% involved a new indication, and 82.2% were considered follow-on products that introduced a new to OTC active ingredient or new dosage form of an already marketed active ingredient to treat an existing OTC indication. A small minority (6.6%) were considered an exceptional innovation that would offer US consumers a genuinely novel OTC product, providing a new to OTC active pharmaceutical ingredient, pharmacological class, and indication. Overall, there was 1 exceptional innovation every 6.7 years. Conclusions Over 40 RTO switches have come to the OTC market in the past 20 years; however, exceptional innovations that expand access to new to OTC active ingredients for new indications are rare. Policies and strategies that result in more innovative switches that can benefit consumers and public health should be evaluated..
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:57 |
---|---|
Enthalten in: |
Therapeutic innovation & regulatory science - 57(2023), 5 vom: 25. Juni, Seite 1074-1080 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Fisher, Matt [VerfasserIn] |
---|
Links: |
Volltext [kostenfrei] |
---|
Themen: |
Consumer healthcare |
---|
Anmerkungen: |
© The Author(s) 2023 |
---|
doi: |
10.1007/s43441-023-00547-9 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
SPR052636771 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | SPR052636771 | ||
003 | DE-627 | ||
005 | 20230804064845.0 | ||
007 | cr uuu---uuuuu | ||
008 | 230804s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1007/s43441-023-00547-9 |2 doi | |
035 | |a (DE-627)SPR052636771 | ||
035 | |a (SPR)s43441-023-00547-9-e | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Fisher, Matt |e verfasserin |4 aut | |
245 | 1 | 2 | |a A Detailed Analysis of the Past 20 Years of US FDA-Approved Prescription to Over-the-Counter Switches |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a Computermedien |b c |2 rdamedia | ||
338 | |a Online-Ressource |b cr |2 rdacarrier | ||
500 | |a © The Author(s) 2023 | ||
520 | |a Objectives This evaluation assesses the quantity, uniqueness, and innovative nature of the past 20 years of Rx-to-OTC (RTO) switches, where a current prescription (Rx) product is reclassified for over-the-counter (OTC) status. Broadening access to more OTC drugs with well-established safety and efficacy could help to reduce healthcare expenditure and address public health challenges. Methods The FDA-maintained RTO switch list website was accessed to generate the primary dataset. Each product listed was assessed for the current OTC availability in the United States of its active ingredient, pharmacological class, and indication to determine its innovative quality. Descriptive statistics were employed in this study. Results From January 2002 through August 2022 there were 45 RTO switches. Among these, 51.1% involved a new to OTC active ingredient, 22.2% involved a new pharmacological class, 6.6% involved a new indication, and 82.2% were considered follow-on products that introduced a new to OTC active ingredient or new dosage form of an already marketed active ingredient to treat an existing OTC indication. A small minority (6.6%) were considered an exceptional innovation that would offer US consumers a genuinely novel OTC product, providing a new to OTC active pharmaceutical ingredient, pharmacological class, and indication. Overall, there was 1 exceptional innovation every 6.7 years. Conclusions Over 40 RTO switches have come to the OTC market in the past 20 years; however, exceptional innovations that expand access to new to OTC active ingredients for new indications are rare. Policies and strategies that result in more innovative switches that can benefit consumers and public health should be evaluated. | ||
650 | 4 | |a FDA |7 (dpeaa)DE-He213 | |
650 | 4 | |a Over-the-counter |7 (dpeaa)DE-He213 | |
650 | 4 | |a Nonprescription |7 (dpeaa)DE-He213 | |
650 | 4 | |a Rx-to-OTC switch |7 (dpeaa)DE-He213 | |
650 | 4 | |a Consumer healthcare |7 (dpeaa)DE-He213 | |
700 | 1 | |a Rawal, Kapil |0 (orcid)0000-0003-0985-1015 |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Therapeutic innovation & regulatory science |d [New York] : Springer Nature, 2013 |g 57(2023), 5 vom: 25. Juni, Seite 1074-1080 |w (DE-627)SPR038904640 |w (DE-600)2708397-4 |x 2168-4804 |7 nnns |
773 | 1 | 8 | |g volume:57 |g year:2023 |g number:5 |g day:25 |g month:06 |g pages:1074-1080 |
856 | 4 | 0 | |u https://dx.doi.org/10.1007/s43441-023-00547-9 |z kostenfrei |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_SPRINGER | ||
951 | |a AR | ||
952 | |d 57 |j 2023 |e 5 |b 25 |c 06 |h 1074-1080 |