» Articles » PMID: 3358900

Pharmaceutical Innovation by the Seven UK-owned Pharmaceutical Companies (1964-1985)

Overview
Specialty Pharmacology
Date 1988 Mar 1
PMID 3358900
Citations 58
Authors
Affiliations
Soon will be listed here.
Abstract

1 A total of three hundred and nineteen new chemical entities (NCEs) were investigated in man for the first time between 1964 and 1985 by seven UK-owned pharmaceutical companies. The majority (96.2%), were self-originated by the UK company or one of its overseas subsidiaries. 2 There was an increase in the number of NCEs investigated each year in man, doubling from an average of 12 per year up to 1980, to over 20 per year between 1981 and 1985. The majority of first drug evaluations in human volunteers were carried out in the UK (92.2%), in contrast to evaluation of new medicines in patients, where 42.9% were first tested outside the UK. 3 The majority of NCEs evaluated in man (78%), were in four therapeutic classes: anti-infectives (32%), anti-allergics (22%), drugs acting on the central nervous system (13%) and cardiovascular system agents (11%). 4 By the end of 1985, 49 (15.4%) of these NCEs had been marketed in the UK and 198 (62.0%) discontinued from further development. The main reasons for termination were inappropriate pharmacokinetics in man (39.4%), and lack of clinical efficacy (29.3%). 5 Average development times increased from less than 2 years between 1964 and 1965, to around 8 years in the 1980s with a consequent reduction in the effective patent life.

Citing Articles

Biopharmaceutical profiling of anti-infective sanggenons from root bark for inhalation administration.

Schwarzinger J, Adelsberger S, Ortmayr K, Stellnberger S, Tahir A, Hadrich G Int J Pharm X. 2024; 8:100272.

PMID: 39252692 PMC: 11381475. DOI: 10.1016/j.ijpx.2024.100272.


Roles of Individual Human Cytochrome P450 Enzymes in Drug Metabolism.

Guengerich F Pharmacol Rev. 2024; 76(6):1104-1132.

PMID: 39054072 PMC: 11549934. DOI: 10.1124/pharmrev.124.001173.


Tools shaping drug discovery and development.

Cheung E, Xia Y, Caporini M, Gilmore J Biophys Rev (Melville). 2024; 3(3):031301.

PMID: 38505278 PMC: 10903431. DOI: 10.1063/5.0087583.


In Silico Screening of Natural Flavonoids against 3-Chymotrypsin-like Protease of SARS-CoV-2 Using Machine Learning and Molecular Modeling.

Cai L, Han F, Ji B, He X, Wang L, Niu T Molecules. 2023; 28(24).

PMID: 38138524 PMC: 10745665. DOI: 10.3390/molecules28248034.


The integrative bioinformatics approaches to predict the xanthohumol as anti-breast cancer molecule: Targeting cancer cells signaling PI3K and AKT kinase pathway.

Gupta K, Sharma K, Chandra H, Panwar H, Bhardwaj N, Altwaijry N Front Oncol. 2023; 12:950835.

PMID: 36591523 PMC: 9798915. DOI: 10.3389/fonc.2022.950835.


References
1.
Mattison N, Thomas E, Trimble A, Wardell W . The development of self-originated new drugs by Swiss pharmaceutical firms, 1960-1980. Regul Toxicol Pharmacol. 1984; 4(2):157-73. DOI: 10.1016/0273-2300(84)90038-2. View

2.
Prentis R, Walker S . Trends in the development of new medicines by UK-owned pharmaceutical companies (1964-1980). Br J Clin Pharmacol. 1986; 21(4):437-43. PMC: 1400936. DOI: 10.1111/j.1365-2125.1986.tb05219.x. View

3.
Wardell W, Hassar M, Anavekar S, Lasagna L . The rate of development of new drugs in the United States, 1963 through 1975. Clin Pharmacol Ther. 1978; 24(2):133-45. DOI: 10.1002/cpt1978242133. View

4.
Speirs C, Griffin J . A survey of the first year of operation of the new procedure affecting the conduct of clinical trials in the United Kingdom. Br J Clin Pharmacol. 1983; 15(6):649-55. PMC: 1427930. DOI: 10.1111/j.1365-2125.1983.tb01545.x. View

5.
Steward F, Wibberley G . Drug innovation--what's slowing it down?. Nature. 1980; 284(5752):118-20. DOI: 10.1038/284118a0. View