Lilly's Kisunla (donanemab-azbt) showed growing benefit over three years in early symptomatic Alzheimer's disease
Data underscores the value of early intervention and supports a limited duration dosing approach with sustained long-term benefits
INDIANAPOLIS, July 30, 2025 /PRNewswire/ -- Eli Lilly and Company (NYSE: LLY) announced results from the long-term extension (LTE) of the Phase 3 TRAILBLAZER-ALZ 2 study showing that participants treated with Kisunla (donanemab-azbt) demonstrated slowing of decline, a benefit that continued to grow over three years compared to an untreated external cohort from the Alzheimer's Disease Neuroimaging Initiative (ADNI).1
Participants in the study who started treatment later still saw benefit. However, earlier initiation of Kisunla in study participants significantly reduced the risk of progression to the next stage of the disease compared to those who received Kisunla treatment later.1 These data were shared as a late breaking 2025 Alzheimer's Association International Conference (AAIC) presentation in Toronto.
'The TRAILBLAZER-ALZ 2 long-term extension reaffirms that Kisunla delivered sustained clinical benefit that continued to increase over three years and a consistent safety profile,' said Mark Mintun, M.D., group vice president, Neuroscience Research & Development, Eli Lilly and Company. 'Participants continued to show meaningful outcomes, reinforcing the long-term value of early intervention.'
The TRAILBLAZER-ALZ 2 LTE study was a Phase 3, double-blind extension of the original TRAILBLAZER-ALZ 2 trial, evaluating the efficacy and safety of Kisunla in individuals with early symptomatic Alzheimer's disease.1 Participants originally treated with Kisunla either continued treatment or were switched to placebo, while those initially on placebo began Kisunla in a blinded manner. An external comparator group from ADNI was used to assess outcomes against a matched, untreated population.
Key preliminary results from the TRAILBLAZER-ALZ 2 LTE study include:
Amyloid-related imaging abnormalities (ARIA) with edema/effusion (ARIA-E) and with hemorrhage/with hemosiderin deposition are side effects within the class of amyloid targeting therapies that do not usually cause any symptoms, but serious and life-threatening symptoms can occur. ARIA can be fatal. Carriers of one or two copies of the apolipoprotein E ε4 (ApoE4) gene may be at higher risk of developing Alzheimer's disease and experiencing ARIA. Patients should discuss any safety concerns with their healthcare providers. Kisunla can also cause certain types of allergic reactions, some of which may be serious and life-threatening, that typically occur during infusion or within 30 minutes post-infusion.2,3 Headache is another commonly reported side effect. See the Indication and Safety Summary with Warnings below for additional information.
About TRAILBLAZER-ALZ 2 Long-Term Extension (LTE) Study
Participants in the TRAILBLAZER-ALZ 2 (core) study who completed the 76-week placebo-controlled period were eligible to continue into the participant- and investigator-blinded LTE period, lasting an additional 78 weeks.
The LTE study included multiple treatment arms:
About TRAILBLAZER-ALZ 2 Study and the TRAILBLAZER-ALZ Program
TRAILBLAZER‐ALZ 2 ( NCT04437511 ) is a multicenter, randomized, double-blind, placebo-controlled (PC) Phase 3 trial designed to assess the efficacy and safety of donanemab in participants with early symptomatic Alzheimer's disease.
Lilly continues to study donanemab in multiple clinical trials, including TRAILBLAZER-ALZ 3, which is evaluating the safety and efficacy of donanemab in patients with preclinical Alzheimer's disease to determine if it reduces risk of progression to symptomatic Alzheimer's disease. TRAILBLAZER-ALZ 5 is a registration trial for early symptomatic Alzheimer's disease currently enrolling in China, Korea, Taiwan, and other geographies. The TRAILBLAZER-ALZ 6 study recently completed the 18-month final study endpoint. Data from the study showed that a modified titration dosing schedule reduced the risk of ARIA-E compared to the TRAILBLAZER-ALZ 2 dosing regimen. These findings supported the FDA approval of an update to the U.S. prescribing information for Kisunla. This data was also presented at AAIC.
INDICATION AND SAFETY SUMMARY WITH WARNINGS
Kisunla (donanemab-azbt), pronounced kih-SUHN-lah, is used to treat adults with early symptomatic Alzheimer's disease (AD), which includes mild cognitive impairment (MCI) or mild dementia stage of disease.
Warnings - Kisunla can cause Amyloid-Related Imaging Abnormalities or 'ARIA.' This is a common side effect that does not usually cause any symptoms, but serious symptoms can occur. ARIA can be fatal. ARIA is most commonly seen as temporary swelling in an area or areas of the brain that usually goes away over time. Some people may also have spots of bleeding on the surface of or in the brain and infrequently, larger areas of bleeding in the brain can occur. Although most people do not have symptoms, some people have headaches, dizziness, nausea, difficulty walking, confusion, vision changes and seizures.
Some people have a genetic risk factor (homozygous apolipoprotein E ε4 gene carriers) that may cause an increased risk for ARIA. Talk to your healthcare provider about testing to see if you have this risk factor.
You may be at higher risk of developing bleeding in the brain if you take medicines to reduce blood clots from forming (antithrombotic medicines) while receiving Kisunla. Talk to your healthcare provider to see if you are on any medicines that increase this risk.
Your healthcare provider will do magnetic resonance imaging (MRI) brain scans before and during your treatment with Kisunla to check you for ARIA. You should carry information that you are receiving Kisunla, which can cause ARIA, and that ARIA symptoms can look like stroke symptoms.
Call your healthcare provider or go to the nearest hospital emergency room right away if you have any of the symptoms listed above.
There are registries that collect information on treatments for Alzheimer's disease. Your healthcare provider can help you become enrolled in these registries.
Warnings - Kisunla can cause serious allergic and infusion-related reactions. Do not receive Kisunla if you have serious allergic reactions to donanemab-azbt or any of the ingredients in Kisunla. Symptoms may include swelling of the face, lips, mouth, or eyelids, problems breathing, hives, chills, irritation of skin, nausea, vomiting, sweating, headache, or chest pain. You will be monitored for at least 30 minutes after you receive Kisunla for any reaction. Tell your healthcare provider right away if you have these symptoms or any reaction during or after a Kisunla infusion.
Other common side effects
Tell your healthcare provider right away if you have any side effects. These are not all of the possible side effects of Kisunla. You can report side effects at 1-800-FDA-1088 or www.fda.gov/medwatch.
Before you receive Kisunla, tell your healthcare provider:
How to receive Kisunla
Kisunla is a prescription medicine given through an intravenous (IV) infusion using a needle inserted into a vein in your arm. Kisunla is given once every 4 weeks. Each infusion will last about 30 minutes.
Learn more
For more information about Kisunla, call 1-800-LillyRx (1-800-545-5979) or go to kisunla.lilly.com.
This summary provides basic information about Kisunla. It does not include all information known about this medicine. Read the information given to you about Kisunla. This information does not take the place of talking with your healthcare provider. Be sure to talk to your healthcare provider about Kisunla. Your healthcare provider is the best person to help you decide if Kisunla is right for you.
Please see full Prescribing Information including boxed warning for ARIA and Medication Guide for Kisunla.
Trademarks and Trade Names
All trademarks or trade names referred to in this press release are the property of the company, or, to the extent trademarks or trade names belonging to other companies are references in this press release, the property of their respective owners. Solely for convenience, the trademarks and trade names in this press release are referred to without the ® and ™ symbols, but such references should not be construed as any indicator that the company or, to the extent applicable, their respective owners will not assert, to the fullest extent under applicable law, the company's or their rights thereto. We do not intend the use or display of other companies' trademarks and trade names to imply a relationship with, or endorsement or sponsorship of us by, any other companies.
About Lilly
Lilly is a medicine company turning science into healing to make life better for people around the world. We've been pioneering life-changing discoveries for nearly 150 years, and today our medicines help tens of millions of people across the globe. Harnessing the power of biotechnology, chemistry and genetic medicine, our scientists are urgently advancing new discoveries to solve some of the world's most significant health challenges: redefining diabetes care; treating obesity and curtailing its most devastating long-term effects; advancing the fight against Alzheimer's disease; providing solutions to some of the most debilitating immune system disorders; and transforming the most difficult-to-treat cancers into manageable diseases. With each step toward a healthier world, we're motivated by one thing: making life better for millions more people. That includes delivering innovative clinical trials that reflect the diversity of our world and working to ensure our medicines are accessible and affordable. To learn more, visit Lilly.com and Lilly.com/news, or follow us on Facebook, Instagram and LinkedIn. P-LLY
Cautionary Statement Regarding Forward-Looking Statements
This press release contains forward-looking statements (as that term is defined in the Private Securities Litigation Reform Act of 1995) about Kisunla (donanemab-azbt) as a treatment for people with early symptomatic Alzheimer's disease, and regulatory approval and other milestones relating to Kisunla and reflects Lilly's current beliefs and expectations. However, as with any pharmaceutical product, there are substantial risks and uncertainties in the process of drug research, development, and commercialization. Among other things, there is no guarantee that planned or ongoing studies will be completed as planned, that future study results will be consistent with study findings to date, that Kisunla will receive additional regulatory approvals or that Kisunla will be commercially successful. For further discussion of these and other risks and uncertainties, see Lilly's Form 10-K and Form 10-Q filings with the United States Securities and Exchange Commission. Except as required by law, Lilly undertakes no duty to update forward-looking statements to reflect events after the date of this release.
References
View original content to download multimedia: https://www.prnewswire.com/news-releases/lillys-kisunla-donanemab-azbt-showed-growing-benefit-over-three-years-in-early-symptomatic-alzheimers-disease-302516488.html
SOURCE Eli Lilly and Company
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Medscape
27 minutes ago
- Medscape
These Two Simple Interventions May Cut CRC Recurrence Risk
This transcript has been edited for clarity. Hello. I'm Dr David Johnson, professor of medicine and chief of gastroenterology at Eastern Virginia Medical School and Old Dominion University in Norfolk, Virginia. New guidelines have lowered the age to begin screening for colon cancer to 45 years old. Although this change is positive, we're still seeing advanced cancer in younger patients who haven't been screened in time. Once diagnosed, these patients undergo surgery and chemotherapy and often return to us asking, 'What can I do now to help myself?' Two recent studies highlight interventions that are simple, affordable, and actionable today: exercise and aspirin. Let's take a closer look at the results. Exercise's Risk Reduction Potential The idea that exercise reduces cancer recurrence and mortality is supported by observational data. The mechanistic effects behind this have been ascribed to metabolic growth factors, inflammatory changes, immune function changes, and perhaps even positive impact on sleep. A study just published in The New England Journal of Medicine examined structured exercise after adjuvant chemotherapy for colon cancer. The phase 3 randomized CHALLENGE trial, mostly conducted at Canadian and Australian centers, recruited patients with resected stage II or III colon cancer (9.8% and 90.2%, respectively) who had completed adjuvant chemotherapy. Patients with recurrences within a year of diagnosis were excluded, as they were more likely to have highly aggressive, biologically active disease. Patients were randomized to receive healthcare education materials alone or in conjunction with a structured exercise program over a 3-year follow-up period. The exercise intervention, delivered in person or virtually, focused on increasing recreational aerobic activity over baseline by at least 10 metabolic equivalent task (MET). An increment of 10 MET hours per week is not too vigorous. It is essentially the equivalent of adding about 45-60 minutes of brisk walking or 25-30 minutes of jogging 3-4 times a week. Patients were asked to increase MET over the first 6 months and then maintain or further increase the amount over the next 2.5 years. They were permitted to structure their own exercise program by choosing the type, frequency, intensity, and duration of aerobic exercise. The primary endpoint was disease-free survival, with secondary endpoints assessing overall survival, patient-reported outcomes, and other outcomes. Although designed to detect differences at 3 years, follow-up was also performed out to 5 and 8 years. At a median follow-up of 7.9 years, exercise reduced the relative risk of disease recurrence, new primary cancer, or death by 28% ( P =.02). This benefit persisted — and even strengthened — over time, with disease-free survival increasing by 6.4 and 7.1 percentage points at 5 and 8 years, respectively. Musculoskeletal adverse events were slightly higher in the exercise group compared with the health education group (18.5% vs 11.5%, respectively), but only 10% were directly attributed to the exercise. There are considerations when interpreting these results. First, there was an attrition over time for compliance and training. It would be interesting to see whether that impacted the results. Second, it's unclear whether patient pedigree or a genomic pathway may predispose to a benefit here for the exercise group. But overall, this phase 3 trial provides class 1 evidence supporting exercise as a low-cost, high-impact intervention to reduce cancer recurrence. Adjuvant Aspirin in Colon Cancer Subset That's a perfect segue into another recent study looking at the effects of adjuvant aspirin on the prevention of recurrence. The ALASCCA trial— conducted across centers in Sweden, Denmark, Finland, and Norway — assessed patients with stage I-III rectal cancer or stage II-III colon cancer. It focused on a subset of patients with an oncogenic abnormality called PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha). PIK3CA occurs in approximately a third of colon cancers and is associated with significant chemotherapy resistance and a higher rate of disease progression. Of the included patients, 1103 (37%) had alterations in the PIK3CA pathway. Researchers randomized patients to receive either 160 mg of aspirin or placebo daily for 3 years, starting within 3 months of surgery. Among patients with PIK3CA mutations, aspirin dramatically reduced the risk for time to recurrence by nearly 50% at 3 years ( P =.044). Adverse events associated with aspirin were minimal, including one case each of gastrointestinal bleeding, hematoma, and allergic reaction. There is no evidence that higher aspirin doses provide greater prevention of colorectal cancer recurrence. The 160 mg use in the current study is fairly normal, roughly equivalent to two low-dose (81 mg) aspirin tablets. Now, it's worth noting that the use of aspirin for the primary prevention of cardiovascular disease was initially recommended by the US Preventive Task Services Force in 2016. This recommendation was then recanted in 2022, when the same group reported limited net benefit to this approach. Two Proactive Actions These studies highlight two interventions — exercise and aspirin — that are low cost, accessible, and appeal to patients eager to help prevent their cancer from recurring. Exercise is broadly beneficial and can be recommended immediately. For aspirin, patients should work with their oncologist to determine their PIK3CA mutation status, as this subgroup appears to benefit the most. These findings offer patients meaningful, proactive interventions they can apply to support their recovery and reduce the risk of recurrence. Hopefully these new findings will help guide your clinical conversations. I'm Dr David Johnson. Thanks for listening.
Yahoo
32 minutes ago
- Yahoo
What is Lyme disease, and does Justin Timberlake have it?
Justin Timberlake isn't the only person to recently contract tick-borne Lyme disease. New Jersey had the third-most cases of Lyme disease in the nation as recently as 2022, according to the New Jersey Department of Health. And with Lyme disease outbreaks on the rise throughout the country, here's what you need to know about Lyme disease and steps you can take to protect yourself and your family. What is Lyme disease? Lyme disease is caused by tick bites but isn't spread person-to-person, noted the the New Jersey Department of Health. The Lyme disease-causing ticks thrive in woodsy areas, such as much of New Jersey. What are Lyme disease symptoms? The three stages of Lyme disease have different symptoms, according to PennMedicine: Stage 1: chills; fevers; joint and muscle pain Stage 2: Nerve numbness; facial paralysis; fainting spells; meningitis Stage 3: fluid buildup in joints; neuropathy How you can prevent, treat Lyme disease The New Jersey Department of Health advises you to avoid wooded areas with dense shrubs and leaf litter, wearing protective clothing, using insect repellents, perform tick checks and mowing lawns frequently will help you avoid tick bites and Lyme disease. "After spending time in tick-infested areas, ask a partner to check you for ticks in areas on your body that you can't see very well," advised the Harvard Medical School. "The common bite areas are the back of the knee, the groin, under the arms, under the breasts in women, behind the ears, and at the back of the neck." Justin Timberlake confirms Lyme disease diagnosis Superstar pop singer Justin Timberlake told his fans in an instagram post that his Lyme disease diagnosis nearly forced him off tour. "Among other things, I've been battling some health issues, and was diagnosed with Lyme disease - which I don't say so you feel bad for me - but to shed some light on what I've been up against behind the scenes," read a portion of Timberlake's lengthy Instagram post. "If you've experienced this disease or know someone who has, then you're aware: living with this can be relentlessly debilitating, both mentally and physically. "When I first got the diagnosis I was shocked for sure. But, at least I could understand why I would be onstage and in a massive amount of nerve pain or, just feeling crazy fatigue or sickness," Timberlake's post continued. "I was faced with a personal decision. Stop touring? Or, keep going and figure it out. I decided the joy that performing brings me far outweighs the fleeting stress my body was feeling. I'm so glad I kept going." According to Business Insider, Timberlake is just the most recent celebrity to come down with Lyme disease. In 2020, both Justin Bieber and Amy Schumer reportedly confirmed their Lyme disease diagnosis, and Avril Lavigne was reportedly bedridden by Lyme disease in 2014. Damon C. Williams is a Philadelphia-based journalist reporting on trending topics across the Mid-Atlantic Region. This article originally appeared on What is Lyme disease, and did Justin Timberlake say he had it? Solve the daily Crossword
Yahoo
an hour ago
- Yahoo
After a Long Day of Travel, She Woke Up Unable to Walk. Then Crawled to Her Car and Drove to the ER (Exclusive)
Ella Katenkamp opens up to PEOPLE about the week she spent in the hospital, the unexpected condition that sidelined her, and what she wishes others understoodNEED TO KNOW Ella Katenkamp was days from finishing school when she woke up unable to walk At first, she assumed the pain in her calves was from working out after a long trip A week later, she left the hospital with a diagnosis that changed how she views her healthElla Katenkamp was days away from finishing school when she woke to a sharp, searing pain in her calves, her feet curled into a locked position and muscles frozen. What followed was a weeklong hospital stay, a terrifying diagnosis and a viral TikTok that sparked a conversation amongst millions. 'I took a trip the week before to Georgia, and it was a lot of, like, hiking,' Katenkamp tells PEOPLE, looking back on what seemed like a fun getaway before things spiraled. 'On the last day, we did a hike with thousands of stairs, and then I drove 13 hours straight back to Florida.' The former college athlete wasted no time jumping back into her routine. 'As soon as I got back, I did a leg workout at the gym,' she says, noting that cramps didn't seem like a big deal at first. 'I got, like, really bad calf pain after that,' she explains. 'My feet locked into a pointed toe position, and I couldn't walk flat-footed. My calves were stuck like that.' Assuming it was a standard athletic cramp, Katenkamp drank water, stretched, and went to bed. But by 5 a.m., the pain was excruciating, and her legs refused to move. 'I lived with a roommate at the time, but it was, like, five in the morning and I didn't want to wake her up,' she says. 'So I crawled to my car and drove myself to the hospital.' At the ER, her condition worsened. 'As soon as I got in there, they ran over and put me in a wheelchair, and that was it for about a week,' she recalls. Throughout her hospital stay, walking was nearly impossible. 'If I walked at all, someone had to hold me up because I couldn't move my calves,' she says. 'They just stopped working.' Doctors struggled to identify the cause of her symptoms. 'It took them about three or four days to figure it out,' Katenkamp notes. 'The nurses would come in and just be Googling my symptoms — no one knew what it was.' Eventually, she received a diagnosis: rhabdomyolysis, a rare condition that causes muscle fibers to break down and release toxins into the blood. 'It's like the breakdown of your muscle to the point that it poisons your blood,' she explains. Katenkamp was shocked to learn her creatine kinase (CK) level, a marker of muscle breakdown, was well above normal. 'Your CK level's not really supposed to be above 200, and when I got to the hospital, it was in the thousands,' she says. Treatment involved flushing her system with fluids and monitoring her blood multiple times a day. 'They had to take my blood like three times a day,' she says. 'After two days, my CK level actually went up, which was really frustrating.' By the time she was discharged, her CK level was still around 600–700. 'I wasn't where I was supposed to be, but I was starting to walk again,' she says. 'It was just my legs.' Doctors attributed the onset to a combination of factors. 'They told me it was probably from the Red Bulls I drank in Georgia, not enough water, my birth control and going from sitting for 13 hours straight into an intense leg workout,' Katenkamp says. The experience permanently changed her approach to fitness and health. 'I took a huge step back from energy drinks,' she shares. 'I didn't touch them for a long time, and now I only drink them very moderately.' Once hyperactive with early-morning practices, classes and games, Katenkamp is now far more mindful. 'I drink so much more water now,' she says. 'And I definitely think about what days to go hard in the gym — like, was I sitting a lot the day before?' The condition was new to her and to many. 'I had no idea what it was,' Katenkamp says. 'Even the doctors didn't know.' She posted about the ordeal on TikTok, with the text overlay, 'She doesn't know it yet... but the next morning she was gonna crawl out of bed on all 4s and drive herself to the hospital at 6am to stay for the next week because her legs were paralyzed with rhabdomyolysis.' While some followers offered support, others jumped to conclusions. But for Katenkamp, it was a moment that turned criticism into community. 'I didn't even really have to defend myself,' she says. 'Other people did it for me.' Many shared their own experiences or those of loved ones. 'A lot of people said they'd been through something similar and knew how painful it was,' she says. 'There were tons of comments wishing me a good recovery.' Looking back, she says the condition was more than just muscle cramps. 'My legs weren't even the same size when I left the hospital,' she says. 'It's definitely a process, but luckily, I'm past it now.' Still, the risk of lasting damage was real. 'They say it can ruin your kidneys,' Katenkamp says. 'Luckily, I didn't get to that point, but if I hadn't gone to the hospital, it could have destroyed my organs.' That's why her message is firm. 'It's more than just cramps,' she says. 'People kept saying, 'Push through it,' but I couldn't have done that — I had to go to the hospital.' Two years later, Katenkamp's advice to others in recovery is simple and compassionate. 'Make sure you're taking care of yourself and read your body,' she says. 'Keep up with your water, stretch and don't overdo it.' She encourages anyone experiencing similar symptoms to investigate all possibilities. 'Follow the steps your doctors give you,' Katenkamp adds. 'It can definitely come back.' Never miss a story — sign up for to stay up-to-date on the best of what PEOPLE has to offer, from celebrity news to compelling human interest stories. If she could tell social media users one thing, it's this: don't pretend to be an expert. 'You never know what's going on,' she says. 'There were over 20 different comments guessing the cause. It's different for every person.' Katenkamp says she understands the appeal of quick judgments, especially online. But she hopes her story shows why empathy matters. 'Don't speak on other people's health,' she says. 'If there's one thing I learned, it's that you really don't know what someone's going through.' Read the original article on People Solve the daily Crossword