Donanemab
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Humanized (from mouse) |
| Target | Amyloid beta |
| Clinical data | |
| Trade names | Kisunla |
| Other names | LY3002813, donanemab-azbt |
| AHFS/Drugs.com | Monograph |
| License data | |
| Routes of administration | Intravenous |
| ATC code | |
| Legal status | |
| Legal status | |
| Identifiers | |
| CAS Number | |
| DrugBank | |
| UNII | |
| KEGG | |
| Chemical and physical data | |
| Formula | C6452H10038N1708O2013S42 |
| Molar mass | 145089.74 g·mol−1 |
Donanemab, sold under the brand name Kisunla, is a monoclonal antibody used for the treatment of Alzheimer's disease.[1][2] Donanemab was developed by Eli Lilly and Company.[3][4]
The most common side effects include amyloid-related imaging abnormalities and headache.[2]
Donanemab was approved for medical use in the United States in July 2024 by the Food and Drug Administration.[2] Treatment is intended for patients with mild cognitive impairment or mild dementia stage of disease, which is the same population the treatment was studied in the clinical trials.[5]
Medical uses
[edit]Donanemab is indicated for the treatment of Alzheimer's disease for people with mild cognitive impairment or mild dementia stage of disease.[2]
Adverse effects
[edit]The US Food and Drug Administration (FDA) label for donanemab contains a boxed warning about amyloid-related imaging abnormalities.[1]
Side effects may include infusion-related reactions, with symptoms such as flu-like symptoms, nausea, vomiting and changes in blood pressure, and hypersensitivity reactions, including anaphylaxis (severe, life-threatening allergic reaction) and angioedema (swelling).[2]
Cerebral edema
[edit]In larger doses of donanemab, some people developed a form of cerebral edema (brain swelling) called "amyloid-related imaging abnormalities with edema or effusions" (ARIA-E); some of these people were asymptomatic while others displayed edema.[6]
Donanemab and Aβ peptide
[edit]Improvements in amyloid imaging technology have linked the excess Aβ peptide outside the cell with the development of Alzheimer's disease.[4] The overproduction of the Aβ peptide creates a plaque in certain parts of the brain, disrupting neurotransmission.[7] Donanemab attacks the soluble and insoluble plaque buildup, slowing the progression of the disease.[8]
History
[edit]The efficacy of donanemab was evaluated in a double-blind, placebo-controlled, parallel-group study (study 1, NCT04437511/TRAILBLAZER-ALZ 2)[9] in participants with Alzheimer’s disease.[2] The participants had confirmed presence of amyloid pathology and mild cognitive impairment or mild dementia stage of disease. 1736 participants were randomized 1:1 to receive 700 mg donanemab every four weeks for the first three doses, and then 1400 mg every four weeks (N = 860) or placebo (N = 876) for a total of up to 72 weeks.[2] The treatment was switched to placebo based on a pre-specified reduction in amyloid levels measured by positron emission tomography (PET) at weeks 24, 52, and 76.[2]
Donanemab has shown positive results in its first trials.[3][6]
Phase I
[edit]First study
[edit]In the United States and Japan, Eli Lilly ran the phase I study from May 2013 to August 2016.[10] The study was conducted on people with mild Alzheimer's disease shown through a positive amyloid PET scan that was conducted on each individual. 100 participants were injected intravenously with donanemab up to four times monthly. Phase I was part of a multi-armed study that used one control group across the different trials. The positive result indicated that the participants had excess amyloid protein in the brain depicting an early sign of Alzheimer's disease. Each month, doses of 0.1 mg/kg to 10 mg/kg were injected into males and non-fertile females at an average age of 74.[11]
Lilly revealed that there were adverse effects for the 37 people who received the treatment and 12 volunteers who received the placebo. The highest dose of donanemab reduced the effect of the plaque burden in the brain.[10] An overall finding was that the higher dosage led to 40% reduction in protein plaques in the brain.
Side effects
[edit] |
Up to four injections occurred monthly until adverse effects led Lilly to alter the trial, increasing the number of injections up to 8 per month and increasing the dosage of patients from 0.1 mg/kg to 0.3 mg/kg. The change in dosages was in conjunction with the decrease in participants from 37 documented volunteers to 9 participants with results available to the public.
There were no adverse symptoms when they were given a singular dose. Donanemab was found to be highly immunogenic, creating an immune response that increases the efficiency of the original antibody infused. In the next part of the trial, where patients received multiple doses, six patients had an infusion reaction which included chills, flushing, dizziness, rash, and fever. No patients had ARIA-E, but there were cases of ARIA-H leaving small hemorrhages in the brain. The two cases with ARIA-H were asymptomatic. Most people developed anti-drug antibodies lowering the drug's effectiveness, with a short half-life of ten days.
Second study
[edit]The second phase I study was conducted in December 2015 in the United States and Japan.[10] This trial had 150 participants, increasing the sample size by 50 people. The method was altered in comparison with the first study conducted. This trial used three different dosing regimens: one with a single dosage of 10, 20, or 40 mg/kg, another with 10 mg/kg every other week for 24 weeks, and a third with 10 or 20 mg/kg every month for 16 months. The participants were randomly selected to be a part of either the placebo group or the real trial, with a ratio of 3:1. The aim of this trial was the same as the first, primarily measuring the effectiveness on reducing amyloid brain plaques.[10]
Side effects
[edit]The increase in dosage led to a larger percentage of participants experiencing symptomatic ARIA-E, rising to 1 in 4 participants. Auto-antibodies were also becoming problematic for donanemab, recognizing the drug as a non-self cell leading to the body fighting against the drug. Anti-drug antibodies, which fall under auto-antibodies were produced in nearly every patient. While this trial showed a positive outcome for participants taking monthly doses for 16 months as the amyloid PET scan became negative, the trial ended in August 2019.[3]
Trailblazer-alz
[edit]The phase II trial methodically differed from phase I, altering the duration, the amount of donanemab, and the number of patients. There was an increase in the amount of donanemab infused into the blood every month for 72 weeks. The patients infused with donanemab and infused with the placebo became equal, creating close to a 1:1 ratio with 257 patients in total.[3] For the first three doses 700 mg was infused and 1400 mg of donanemab for every dose after that. A PET scan was also used to measure the amount of plaque in the brain. TRAILBLAZER-ALZ was the method used to improve the placebo-controlled group as it was randomised. It assessed the safety and efficacy of donanemab.[10]
It consisted of a trial combining two experimental drugs under Lilly that target separate parts of the amyloid cascade. The goal of this phase II trial was to see how safe, tolerable, and effective an 18-month term of donanemab alone and in combination with Lilly's BACE inhibitor LY3202626.[10] This BACE inhibitor was administered orally compared to donanemab which is intravenously injected. To effectively see the comparison between patients only taking donanemab and patients taking both of Lily's drugs was effectively achieved by studying three separate groups. One group had donanemab injections and orally received Lilly's BACE inhibitor, another had only donanemab injections, and the third was the placebo group. It planned to enroll 375 people whose memories had been deteriorating for at least six months and who scored above a certain threshold on the CogState Bridging Test but ended up with 257 participants.
Results
[edit]There was a reduction in plaque level which was highlighted through improved cognition and ability to perform daily activities. Phase II showed promising results at the beginning without analyzing its effects and the data in detail. It was concluded that there was no substantial difference in the results between the placebo group and the patients infused with donanemab. After phase II, the trial was stopped.[10]
Side effects
[edit]There was an overview on the adverse drug reactions (iADRS) when taking donanemab and the scores were similar to the placebo group, showing no significant difference. There were cases of ARIA-E but only asymptomatic which is an improvement from the symptomatic patients seen in phase I.[3] Lilly decided to continue trials for donanemab but discontinue the trials with the BACE inhibitor in October in 2018. In 2021 the TRAILBLAZER-ALZ trial was completed, indicating the current success of donanemab as it slows down the development of Alzheimer's disease; but with the side effects still being problematic, further investigation was needed.
Phase III
[edit]In October and November 2020, Lilly extended the TRAILBLAZER-ALZ to have a second study. It was run with 87 sites across Canada, the Netherlands, and Poland.[10]
In May 2023, the company reported its phase III study showed the drug could slow the pace of Alzheimer's disease by 35%.[12] In July 2023, results from 1,736 people treated with donanemab showed slowing of Alzheimer's progression at 76 weeks, with 24% of the people displaying cerebral edema.[6]
Society and culture
[edit]Legal status
[edit]In July 2024, donanemab was approved for medical use in the United States.[2][13][14] The U.S. Food and Drug Administration (FDA) granted the application for donanemab fast track, priority review, and breakthrough therapy designations.[2]
In October 2024, donanemab was approved for medical use in the United Kingdom by the Medicines and Healthcare products Regulatory Agency.[15]
Economics
[edit]The list price for donanemab is US$32,000 for a course of therapy lasting a year.[16]
Names
[edit]Donanemab is the international nonproprietary name.[17]
References
[edit]- ^ a b c "Kisunla- donanemab-azbt injection, solution". DailyMed. 2 July 2024. Retrieved 15 August 2024.
- ^ a b c d e f g h i j k "FDA approves treatment for adults with Alzheimer's disease". U.S. Food and Drug Administration (FDA) (Press release). 2 July 2024. Archived from the original on 2 July 2024. Retrieved 2 July 2024.
This article incorporates text from this source, which is in the public domain.
- ^ a b c d e Mintun MA, Lo AC, Duggan Evans C, Wessels AM, Ardayfio PA, Andersen SW, et al. (May 2021). "Donanemab in Early Alzheimer's Disease". The New England Journal of Medicine. 384 (18): 1691–1704. doi:10.1056/NEJMoa2100708. PMID 33720637.
- ^ a b Long JM, Holtzman DM (October 2019). "Alzheimer Disease: An Update on Pathobiology and Treatment Strategies". Cell. 179 (2): 312–339. doi:10.1016/j.cell.2019.09.001. PMC 6778042. PMID 31564456.
- ^ "FDA approves treatment for Alzheimer's disease - The Yucatan Times". 12 July 2024. Retrieved 15 July 2024.
- ^ a b c Sims JR, Zimmer JA, Evans CD, Lu M, Ardayfio P, Sparks J, et al. (August 2023). "Donanemab in Early Symptomatic Alzheimer Disease: The TRAILBLAZER-ALZ 2 Randomized Clinical Trial". JAMA. 330 (6): 512–527. doi:10.1001/jama.2023.13239. PMC 10352931. PMID 37459141.
- ^ Demattos RB, Lu J, Tang Y, Racke MM, Delong CA, Tzaferis JA, et al. (December 2012). "A plaque-specific antibody clears existing β-amyloid plaques in Alzheimer's disease mice". Neuron. 76 (5): 908–20. doi:10.1016/j.neuron.2012.10.029. PMID 23217740. S2CID 16620402.
- ^ Gallardo G, Holtzman DM (2019). "Amyloid-β and Tau at the Crossroads of Alzheimer's Disease". Tau Biology. Advances in Experimental Medicine and Biology. Vol. 1184. pp. 187–203. doi:10.1007/978-981-32-9358-8_16. ISBN 978-981-32-9357-1. PMID 32096039. S2CID 211476346.
- ^ "A Study of Donanemab (LY3002813) in Participants With Early Alzheimer's Disease (TRAILBLAZER-ALZ 2)". ClinicalTrials.gov. Retrieved 2 July 2024.
- ^ a b c d e f g h "Donanemab Confirms: Clearing Plaques Slows Decline—By a Bit". AlzForum Foundation. 2021. Archived from the original on 23 April 2021. Retrieved 23 April 2021.
- ^ Lowe SL, Willis BA, Hawdon A, Natanegara F, Chua L, Foster J, et al. (2021). "Donanemab (LY3002813) dose-escalation study in Alzheimer's disease". Alzheimer's & Dementia. 7 (1): e12112. doi:10.1002/trc2.12112. PMC 7882532. PMID 33614890.
- ^ "Eli Lilly Alzheimer's treatment donanemab slowed disease progression in clinical trial". CNBC. 3 May 2023. Archived from the original on 3 May 2023. Retrieved 3 May 2023.
- ^ "Notable Approvals". U.S. Food and Drug Administration (FDA). 2 July 2024. Archived from the original on 13 June 2024. Retrieved 3 July 2024.
- ^ "Lilly's Kisunla (donanemab-azbt) Approved by the FDA for the Treatment of Early Symptomatic Alzheimer's Disease" (Press release). Eli Lilly. 2 July 2024. Archived from the original on 2 July 2024. Retrieved 2 July 2024 – via PR Newswire.
- ^ "New Alzheimer's drug, donanemab – what is it and how does it work?". Alzheimer's Research UK. 23 October 2024. Retrieved 23 October 2024.
- ^ Belluck P (2 July 2024). "New Drug Approved for Early Alzheimer's". The New York Times. Archived from the original on 2 July 2024. Retrieved 3 July 2024.
- ^ World Health Organization (2019). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 82". WHO Drug Information. 33 (3). hdl:10665/330879.
External links
[edit]- "Donanemab (Code C166484)". NCI Thesaurus.
