» Articles » PMID: 32151051

2019 FDA TIDES (Peptides and Oligonucleotides) Harvest

Overview
Publisher MDPI
Specialty Chemistry
Date 2020 Mar 11
PMID 32151051
Citations 35
Authors
Affiliations
Soon will be listed here.
Abstract

2019 has been an excellent year in terms of peptides and oligonucleotides (TIDES) approved by the FDA. Despite the drop in the number of total drugs approved by the FDA in 2019 in comparison with 2018 (48 vs. 59), the total number of TIDES authorized increased (seven vs. three). Year after year, TIDES are increasingly present in therapy, as imaging agents, theragnostic and constituent moieties of other complex drugs, such as antibody drug conjugates. This means a consolidation of these kinds of drugs in the pharmaceutical arena, paving the way in the coming years for the approval of others for diverse medical indications. Here the TIDES approved in 2019 are analyzed in terms of chemical structure, medical target, mode of action, and adverse effects.

Citing Articles

FDA-approved drugs featuring macrocycles or medium-sized rings.

Du Y, Semghouli A, Wang Q, Mei H, Kiss L, Baecker D Arch Pharm (Weinheim). 2025; 358(1):e2400890.

PMID: 39865335 PMC: 11771699. DOI: 10.1002/ardp.202400890.


An Improved P(V) Thio-Oligonucleotide Synthesis Platform.

Nassir M, Gherardi L, Redman R, Jin Y, Yao F, Yang Y Org Lett. 2024; 27(1):97-102.

PMID: 39700460 PMC: 11723805. DOI: 10.1021/acs.orglett.4c03980.


Porous silicon and silica carriers for delivery of peptide therapeutics.

Yan J, Siwakoti P, Shaw S, Bose S, Kokil G, Kumeria T Drug Deliv Transl Res. 2024; 14(12):3549-3567.

PMID: 38819767 PMC: 11499345. DOI: 10.1007/s13346-024-01609-7.


Exploring FDA-Approved Frontiers: Insights into Natural and Engineered Peptide Analogues in the GLP-1, GIP, GHRH, CCK, ACTH, and α-MSH Realms.

Al Musaimi O Biomolecules. 2024; 14(3).

PMID: 38540684 PMC: 10968328. DOI: 10.3390/biom14030264.


Peptide-encoding gene transfer to modulate intracellular protein-protein interactions.

Taya T, Kami D, Teruyama F, Matoba S, Gojo S Mol Ther Methods Clin Dev. 2024; 32(2):101226.

PMID: 38516692 PMC: 10952081. DOI: 10.1016/j.omtm.2024.101226.


References
1.
Bargh J, Isidro-Llobet A, Parker J, Spring D . Cleavable linkers in antibody-drug conjugates. Chem Soc Rev. 2019; 48(16):4361-4374. DOI: 10.1039/c8cs00676h. View

2.
Al Shaer D, Al Musaimi O, Albericio F, de la Torre B . 2018 FDA Tides Harvest. Pharmaceuticals (Basel). 2019; 12(2). PMC: 6631726. DOI: 10.3390/ph12020052. View

3.
Miller M, Smith J, Norman J, Clayton A . Expert opinion on existing and developing drugs to treat female sexual dysfunction. Expert Opin Emerg Drugs. 2018; 23(3):223-230. DOI: 10.1080/14728214.2018.1527901. View

4.
Graham M, Gu X, Ginader T, Breheny P, Sunderland J . Ga-DOTATOC Imaging of Neuroendocrine Tumors: A Systematic Review and Metaanalysis. J Nucl Med. 2017; 58(9):1452-1458. PMC: 6944175. DOI: 10.2967/jnumed.117.191197. View

5.
Diamantis N, Banerji U . Antibody-drug conjugates--an emerging class of cancer treatment. Br J Cancer. 2016; 114(4):362-7. PMC: 4815767. DOI: 10.1038/bjc.2015.435. View