Lilly's Taltz (ixekizumab) and Zepbound (tirzepatide) used together delivered superior efficacy in first-of-its-kind Phase 3b trial for adults with psoriasis and obesity or overweight

Rhea-AI Summary

Eli Lilly (NYSE: LLY) reported positive topline 36-week results from the Phase 3b TOGETHER-PsO trial: concomitant Taltz (ixekizumab) plus Zepbound (tirzepatide) met the primary endpoint and all key secondaries versus Taltz alone.

Key results: 27.1% reached PASI 100 plus ≥10% weight loss vs 5.8% (p<0.001); 40.6% achieved PASI 100 vs 29.0% (p<0.05). Mean BMI >39 kg/m2. Adverse events were generally mild to moderate and consistent with known profiles. Detailed 36-week data will be published and discussed with regulators.

Positive

• 27.1% achieved PASI 100 plus ≥10% weight loss (p<0.001)
• PASI 100 rate 40.6% vs 29.0% (Taltz+Zepbound vs Taltz; p<0.05)
• First-of-its-kind data supporting combined biologic plus incretin approach

Negative

• Adverse events included nausea, diarrhea, constipation, vomiting, dizziness
• Open-label Phase 3b design may limit blinded efficacy comparisons

News Market Reaction – LLY

-1.50%

-1.50% Session close to close

In the Feb 18 session, LLY declined 1.50%, reflecting a mild negative market reaction.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement highlights Phase 3b data where Taltz plus Zepbound outperformed Taltz alone, with ...

Analysis

This announcement highlights Phase 3b data where Taltz plus Zepbound outperformed Taltz alone, with PASI 100 plus 10% weight loss in 27.1% vs 5.8% of patients and higher complete clearance rates (40.6% vs 29.0%). It reinforces Lilly’s strategy around obesity and immunology seen in recent earnings and manufacturing expansions. Key factors to watch include full peer-reviewed results, regulatory feedback, real-world tolerability, and how these findings integrate into psoriasis and obesity treatment guidelines.

Key Figures

Primary endpoint result: 27.1% vs 5.8% PASI 100 rates: 40.6% vs 29.0% Trial duration: 36 weeks +5 more

8 metrics

Primary endpoint result 27.1% vs 5.8% PASI 100 plus ≥10% weight loss at 36 weeks, combo vs Taltz alone

PASI 100 rates 40.6% vs 29.0% Patients achieving PASI 100, Taltz+Zepbound vs Taltz monotherapy

Trial duration 36 weeks TOGETHER-PsO Phase 3b concomitant treatment study period

High BMI level more than 39 kg/m² Average BMI across both treatment arms in TOGETHER-PsO

BMI above prior trials 9–10 kg/m² higher Mean BMI vs any prior Phase 3 pivotal psoriasis biologic trial

Extent of skin involvement approximately 25% Average body surface area affected by psoriasis in TOGETHER-PsO

High-impact areas involved 97% of patients Psoriasis affecting face, scalp or genitals in TOGETHER-PsO

Psoriasis with obesity approximately 61% U.S. people with psoriasis who also have obesity or overweight

Historical Context

5 past events · Latest: Feb 17 (Positive)

Pattern 5 events

Date	Event	Sentiment	24h Move	Catalyst
Feb 17	CRISPR partnership milestone	Positive	-0.4%	Second success milestone in in vivo CRISPR collaboration for neuro diseases.
Feb 16	Conference participation	Neutral	-0.4%	Announcement of TD Cowen health care conference fireside chat appearance.
Feb 09	Acquisition announcement	Neutral	-1.3%	Agreement to acquire Orna Therapeutics for up to $2.4B cash.
Feb 04	Earnings and guidance	Positive	+10.3%	Q4 2025 beat with $19.3B revenue and strong 2026 EPS/revenue guidance.
Jan 30	Manufacturing expansion	Positive	+1.3%	Plan to invest > $3.5B in new U.S. injectable manufacturing site.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent news, especially strong earnings and obesity-related investments, has more often aligned with positive price reactions, while at least one partnership milestone saw a negative reaction.

Recent Company History

Over the last few weeks, Lilly has reported strong Q4 2025 earnings with revenue of $19.3B and 2026 guidance of $80–$83B, driving a 10.33% move higher. The company announced a large Pennsylvania manufacturing build (> $3.5B) for weight-loss therapies and an acquisition of Orna Therapeutics (up to $2.4B). A CRISPR partnership milestone and conference participation had smaller or negative moves. Today’s psoriasis/obesity Phase 3b data fits the broader obesity- and immunology-focused growth narrative.

Key Terms

PASI 100, Psoriasis Area Severity Index, monoclonal antibody, interleukin 17A (IL-17A), +4 more

8 terms

PASI 100 medical

"complete skin clearance (PASI 100) and 10% weight loss"

PASI 100 is a clinical-trial measure meaning a patient’s psoriasis has cleared completely, showing a 100% improvement on the Psoriasis Area and Severity Index. Think of it like a before-and-after photo where all visible signs of the condition are gone. For investors, PASI 100 signals a therapy’s top-level effectiveness claim, which can drive regulatory approval prospects, market adoption and a product’s commercial value.

Psoriasis Area Severity Index medical

"Psoriasis Area Severity Index (PASI) 100) and at least 10% weight loss"

Psoriasis Area Severity Index (PASI) is a clinician-scored scale that measures how much of the body is affected by psoriasis and how severe the plaques are, producing a single numerical score like a health “report card” for the skin. Investors care because PASI scores are commonly used in clinical trials and regulatory reviews to show whether a treatment works; stronger, consistent PASI improvements can drive approvals, market adoption, and revenue potential.

monoclonal antibody medical

"Taltz is a monoclonal antibody that selectively binds with interleukin 17A"

A monoclonal antibody is a laboratory-made protein designed to recognize and attach to a specific target in the body, such as a disease-causing substance or cell. It functions like a highly precise lock-and-key tool, helping to treat or detect illnesses. For investors, companies developing monoclonal antibodies can represent promising opportunities in the healthcare sector, especially as these treatments often address unmet medical needs.

interleukin 17A (IL-17A) medical

"selectively binds with interleukin 17A (IL-17A) cytokine and inhibits its interaction"

A small protein messenger produced by certain immune cells that acts like an alarm bell to trigger inflammation. It plays a central role in several autoimmune and inflammatory diseases, so drugs that block or mimic it can reduce symptoms or alter disease progression. Investors watch it because therapies targeting this messenger drive clinical trial activity, regulatory decisions, and potential market value in pharmaceuticals and biotechnology.

GLP-1 medical

"dual GIP (glucose-dependent insulinotropic polypeptide) and GLP-1 (glucagon-like"

GLP-1 (glucagon-like peptide-1) is a natural hormone in the body that helps regulate blood sugar levels and appetite. Its significance to investors lies in its role as the basis for a class of medications that address conditions like type 2 diabetes and obesity, which are large and growing markets. Advances or investments in GLP-1-based treatments can signal opportunities in healthcare innovation and potentially impact pharmaceutical companies’ growth.

GIP medical

"only FDA-approved dual GIP (glucose-dependent insulinotropic polypeptide) and GLP-1"

GIP commonly stands for Global Infrastructure Partners, a private investment firm that buys and manages large physical assets such as airports, power plants, toll roads and pipelines. Investors pay attention because when GIP acquires, invests in, or sells such assets it can alter cash flow, debt levels and long-term plans for those businesses—like a new landlord changing rents or making upgrades—affecting revenue, dividends and risk for shareholders and creditors.

Phase 3b medical

"TOGETHER-PsO open-label Phase 3b clinical trial evaluating the concomitant use"

Phase 3b is an additional clinical trial stage run after the main large-scale efficacy studies but usually before or around regulatory approval; it gathers extra information on safety, dosing, specific patient groups, or real-world use to strengthen understanding of a medicine. For investors, phase 3b studies can change approval details, usage guidelines or market potential—think of them as final rehearsals that can alter the product’s launch plan and commercial prospects.

incretin therapy medical

"comprehensive treatment approach alongside an incretin therapy for people with psoriasis"

Incretin therapy is a medical treatment that helps control blood sugar levels by using hormones that signal the body to release more insulin after eating. It is important to investors because these therapies represent a growing area in diabetes management, potentially driving the success of related pharmaceutical companies and impacting healthcare costs and patient outcomes.

AI-generated analysis. How Rhea-AI works. Not financial advice.

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google

Add on Google Not now

At 36 weeks in the TOGETHER-PsO study, concomitant Taltz and Zepbound met primary endpoint of superiority vs. Taltz monotherapy in achieving complete skin clearance (PASI 100) and ≥10% weight loss

In a key secondary endpoint, patients taking Taltz and Zepbound were 40% more likely to achieve PASI 100 compared to those taking Taltz alone (40.6% of patients vs. 29.0%, p<0.05)

Taltz is the first and only psoriatic disease biologic with data from two trials supporting a potential comprehensive treatment approach alongside an incretin therapy for obesity 

INDIANAPOLIS, Feb. 18, 2026 /PRNewswire/ -- Eli Lilly and Company (NYSE: LLY) today announced positive topline results from the landmark TOGETHER-PsO open-label Phase 3b clinical trial evaluating the concomitant use of Taltz (ixekizumab) and Zepbound (tirzepatide) compared to Taltz alone in adults with moderate-to-severe plaque psoriasis and obesity or overweight with at least one additional weight-related comorbid condition. At 36 weeks, treatment with Taltz and Zepbound met the primary and all key secondary endpoints, delivering superior skin clearance and weight loss versus Taltz monotherapy. In the U.S., approximately 61% of people with psoriasis also have obesity or overweight with at least one weight-related comorbidity,¹ highlighting a need for comprehensive treatment approaches that address the full burden of their diseases.

In the first-of-its-kind TOGETHER-PsO study, 27.1% of participants receiving Taltz and Zepbound reached complete skin clearance (Psoriasis Area Severity Index (PASI) 100) and at least 10% weight loss, compared to 5.8% of patients treated with Taltz alone, meeting the primary endpoint (p<0.001). In a key secondary endpoint, Taltz plus Zepbound delivered a 40% relative increase over Taltz monotherapy in the proportion of patients who achieved PASI 100 (40.6% of patients vs. 29.0%, respectively, p<0.05), demonstrating that treatment of obesity or overweight with Zepbound reduced the burden of psoriasis.²

The study enrolled a population with a very high burden of disease that is often associated with poorer treatment outcomes,³ with an average BMI of more than 39 kg/m² across both treatment arms. This reflects a mean BMI of approximately 9-10 kg/m² higher than any population studied to date in Phase 3 pivotal trials of a psoriasis biologic.^4-9 An increase in BMI has been shown to reduce the odds of reaching skin clearance across multiple psoriasis studies.¹⁰ Most patients in the TOGETHER-PsO trial had extensive skin involvement, with approximately 25% of their body surface area affected, and nearly all (97%) had psoriasis affecting high-impact body areas linked to significant morbidity, itch, and skin pain, such as the face, scalp or genitals.^11,12

"Psoriasis and obesity can profoundly impact how people feel, how they are seen, and how they live," said Adrienne Brown, executive vice president and president, Lilly Immunology. "For people living at the intersection of these chronic inflammatory diseases, these PASI 100 results represent far more than a clinical milestone—they demonstrate what becomes possible when we address both simultaneously. Taltz has a decade of proven efficacy in psoriasis, and the superior outcomes achieved when Zepbound was used concomitantly for obesity signal a potential advance in treatment for patients who deserve nothing less."

Adverse events in participants treated with concomitant administration of Taltz and Zepbound were generally mild to moderate, and the types of adverse events were generally consistent with the known safety profile of each medicine. The most common adverse events occurring in ≥5% of participants were nausea, diarrhea, constipation, injection site reaction, dosing error, vomiting, and dizziness in the Taltz and Zepbound concomitant treatment arm, and injection site reaction, dosing error, and nasopharyngitis in the Taltz monotherapy arm.

"Psoriasis and obesity share underlying inflammatory pathways, yet they are too often treated in silos despite psoriasis treatment guidelines calling for obesity management," said Mark Lebwohl, M.D., Dean for Clinical Therapeutics, and Professor and Chairman Emeritus of the Department of Dermatology at the Icahn School of Medicine at Mount Sinai, and TOGETHER-PsO principal investigator. "This study involved patients with particularly high BMI and difficult-to-treat psoriasis, making the PASI 100 results with Taltz plus Zepbound especially remarkable. The findings show that treating psoriasis and obesity or overweight at the same time significantly improved outcomes, reinforcing psoriasis as an obesity-related condition and supporting a potential comprehensive approach to care."

Taltz is a monoclonal antibody that selectively binds with interleukin 17A (IL-17A) cytokine and inhibits its interaction with the IL-17 receptor. Building on positive topline data from the TOGETHER-PsA study, it is now the only biologic with data supporting a comprehensive treatment approach alongside an incretin therapy for people with psoriasis or psoriatic arthritis who also have obesity or overweight. Zepbound is the only FDA-approved dual GIP (glucose-dependent insulinotropic polypeptide) and GLP-1 (glucagon-like peptide-1) receptor agonist obesity management medication.

Detailed 36-week results from TOGETHER-PsO will be published in a peer-reviewed journal and discussed with regulators.

About the TOGETHER-PsO Trial
TOGETHER-PsO (NCT06588283) is a 52-week Phase 3b, randomized, multicenter, assessor-blinded, open-label study assessing the efficacy and safety of concomitant administration of Taltz and Zepbound compared with Taltz alone in adult participants with moderate-to-severe plaque psoriasis and obesity or overweight with at least one additional weight-related comorbid condition. A total of 274 participants were randomized 1:1 to receive either Taltz alone or concomitantly with Zepbound, both administered subcutaneously. Patients in both arms received counseling on a reduced-calorie diet and increased physical activity. The primary objective of the study is to assess the proportion of participants achieving both Psoriasis Area and Severity Index (PASI) 100 and ≥10% weight reduction at Week 36. Participants must have a BMI ≥30 kg/m², or ≥27 to <30 kg/m² with at least one weight-related comorbidity.

About Taltz (ixekizumab)¹³
Taltz is a monoclonal antibody that selectively binds with interleukin 17A (IL-17A) cytokine and inhibits its interaction with the IL-17 receptor. IL-17A is a naturally occurring cytokine that is involved in normal inflammatory and immune responses. Taltz inhibits the release of pro-inflammatory cytokines and chemokines. Taltz is approved to treat adults and children 6 years and older with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy. Additionally, Taltz is approved for adults with active psoriatic arthritis, adults with active ankylosing spondylitis, and adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation.

About Zepbound (tirzepatide) injection¹⁴
Zepbound is a GIP (glucose-dependent insulinotropic polypeptide) and GLP-1 (glucagon-like peptide-1) receptor agonist obesity medication. Zepbound lowers body weight by decreasing calorie intake and appetite. Zepbound is indicated in combination with a reduced-calorie diet and increased physical activity to reduce excess body weight and maintain weight reduction in adults with obesity, or adults with overweight in the presence of at least one weight-related comorbid condition. Additionally, Zepbound is FDA-approved to treat adults with moderate-to-severe obstructive sleep apnea and obesity in combination with a reduced-calorie diet and increased physical activity. Zepbound contains tirzepatide and should not be used with other tirzepatide-containing products or any GLP-1 receptor agonist medicines. It is not known if Zepbound is safe and effective for use in children.

Endnotes and References
¹ Armstrong et al, Addressing the Obesity-Psoriasis Connection: Prevalence, Incidence, and Comorbidity Insights from a Large US Population of 19.9 Million (2018-2024). Presented at Maui Derm, 2026.
² Hypothetical estimand in the modified intent-to-treat (mITT) population is used. The hypothetical estimand represents efficacy in all mITT participants who remained on study intervention without initiating prohibited medication.
³ Enos, Clinton W. et al. Comorbid obesity and history of diabetes are independently associated with poorer treatment response to biologics at 6 months: A prospective analysis in Corrona Psoriasis Registry. Journal of the American Academy of Dermatology, Volume 86, Issue 1, 68 - 76.
⁴ Lebwohl M, Strober B, Menter A, et al. Phase 3 studies comparing brodalumab with ustekinumab in psoriasis. N Engl J Med. 2015;373(14):1318-1328.
⁵ Langley RG, Elewski BE, Lebwohl M, et al. Secukinumab in plaque psoriasis — results of two phase 3 trials. N Engl J Med. 2014;371(4):326-338.
⁶ Griffiths CE, Reich K, Lebwohl M, et al. Comparison of ixekizumab with etanercept or placebo in moderate-to-severe psoriasis (UNCOVER-2 and UNCOVER-3): results from two phase 3 randomised trials. Lancet. 2015;386(9993):541-551.
⁷ Gordon KB, Strober B, Lebwohl M, et al. Efficacy and safety of risankizumab in moderate-to-severe plaque psoriasis (UltIMMa-1 and UltIMMa-2): results from two double-blind, randomised, placebo-controlled and ustekinumab-controlled phase 3 trials. Lancet. 2018;392(10148):650-661.
⁸ Reich K, Armstrong AW, Langley RG, et al. Guselkumab versus secukinumab for the treatment of moderate-to-severe psoriasis (ECLIPSE): results from a phase 3, randomised controlled trial. Lancet. 2019;394(10201):831-839.
⁹ Gordon KB, Foley P, Krueger JG, et al. Bimekizumab efficacy and safety in moderate to severe plaque psoriasis (BE READY): a multicentre, double-blind, placebo-controlled, randomised withdrawal phase 3 trial. Lancet. 2021;397(10273):475-486.
¹⁰ Hjort G, Schwarz CW, Skov L, Loft N. Clinical characteristics associated with response to biologics in the treatment of psoriasis: a meta-analysis. JAMA Dermatol. 2024;160(8):830-837. DOI: 10.1001/jamadermatol.2024.1677
¹¹ Weight-related comorbidities in study participants included cardiovascular disease, type 2 diabetes mellitus (T2DM), dyslipidemia, hypertension, obstructive sleep apnea (OSA). Participants had an average of 14.6 years since their psoriasis diagnosis. High-impact body areas impacted by psoriasis included the face, genitalia, scalp, palm, sole, axilla, inframammary fold, abdominal skin fold and inguinal region.
¹² Merola JF, Qureshi A, Husni ME. Underdiagnosed and undertreated psoriasis: Nuances of treating psoriasis affecting the scalp, face, intertriginous areas, genitals, hands, feet, and nails. Dermatol Ther. 2018 May;31(3):e12589. doi: 10.1111/dth.12589. Epub 2018 Mar 6. PMID: 29512290; PMCID: PMC6901032.
¹³ Taltz. Prescribing Information. Lilly USA, LLC.
¹⁴ Zepbound. Prescribing Information. Lilly USA, LLC.

TALTZ INDICATIONS AND SAFETY SUMMARY
Taltz^® (tȯl-ts) is an injectable medicine used to treat:

• People 6 years of age and older with moderate to severe plaque psoriasis who may benefit from taking injections or pills (systemic therapy) or treatment using ultraviolet or UV light (phototherapy).
• Adults with active psoriatic arthritis.
• Adults with active ankylosing spondylitis.
• Adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation.

It is not known if Taltz is safe and effective in children for conditions other than plaque psoriasis or in children under 6 years of age.

Warnings - Taltz affects the immune system. It may increase your risk of infections, some people have had serious infections, including tuberculosis (TB), and infections caused by bacteria, fungi, or viruses that can spread throughout the body. Some people have been hospitalized from these infections. Do not use Taltz if you have any symptoms of infection, unless your doctor tells you to. If you have a symptom after starting Taltz, call your doctor right away.

Your doctor should check you for TB before you start Taltz, and watch you closely for signs of TB during and after treatment with Taltz. If you have TB, or had it in the past, your doctor may treat you for it before you start Taltz.

Do not use Taltz if you have had a serious allergic reaction to ixekizumab or any other ingredient in Taltz, such as: swelling of your eyelids, lips, mouth, tongue or throat, trouble breathing, feeling faint, throat or chest tightness, or skin rash. Get emergency help right away if you have any of these reactions. See the Medication Guide that comes with Taltz for a list of ingredients.

Severe skin reactions that look like eczema can happen during treatment with Taltz from days to months after your first dose and can sometimes lead to hospitalization. Your doctor may temporarily stop treatment with Taltz if you develop severe skin reactions. Tell your doctor if you have any of the following: redness or rash, itching, patches, your skin is dry or feels like leather, blisters or abrasions that ooze or become crusty, small bumps or plaques with scale or crusting.

Crohn's disease or ulcerative colitis (inflammatory bowel disease) can start or get worse with Taltz use. Tell your doctor if you have any of these symptoms or if they get worse: stomach pain, diarrhea, and weight loss.

You should not get live vaccines while taking Taltz. You should get the vaccines you need before you start Taltz.

Common side effects
The most common side effects of Taltz include:

• Injection site reactions
• Nausea
• Upper respiratory infections
• Fungal skin infections

Tell your doctor if you have any side effects. You can report side effects at 1-800-FDA-1088 or www.fda.gov/medwatch.

Before using
Before you use Taltz, review these questions with your doctor:

• Are you being treated for an infection?
• Do you have an infection that does not go away or keeps coming back?
• Do you have TB or have you been in close contact with someone with TB?
• Do you have possible symptoms of an infection such as fever, cough, sores, diarrhea, or other symptoms? Ask your doctor about other possible symptoms.
• Do you have Crohn's disease or ulcerative colitis?

Tell your doctor if:

• You need any vaccines or have had one recently.
• You take prescription or over-the-counter medicines, vitamins, or herbal supplements.
• You are pregnant or planning to become pregnant. It is not known if Taltz can harm an unborn baby. 
• Pregnancy Exposure Registry: There is a pregnancy registry to collect information about women who are exposed to Taltz during pregnancy. The purpose of this registry is to collect information about the health of you and your baby. If you become pregnant while taking Taltz, you are encouraged to enroll in the pregnancy registry by calling 1-800-284-1695 or by visiting online at http://www.pregnancyregistry.lilly.com.
• You are breastfeeding or planning to breastfeed. It is not known if Taltz passes into breastmilk.

How to take
See the instructions for use that come with Taltz. There you will find information about how to store, prepare, and inject Taltz. Adults may self-inject after receiving training from a healthcare provider.

For children 6 to 17 years of age:

• If your child's healthcare provider decides that you may give Taltz injections at home, you should receive training on the right way to prepare and inject Taltz. Do not try to give Taltz to your child until you have been shown how to inject Taltz. Children should not inject themselves with Taltz. You or an adult caregiver should prepare and give Taltz injections to your child.

Learn more
Taltz is a prescription medicine available as a 80 mg/mL, 40 mg/0.5mL, 20 mg/0.25mL injection. For more information, call 1-800-545-5979 or go to taltz.lilly.com.

This summary provides basic information about Taltz but does not include all information known about this medicine. Read the information that comes with your prescription each time your prescription is filled. This information does not take the place of talking with your doctor. Be sure to talk to your doctor or other healthcare provider about Taltz and how to take it. Your doctor is the best person to help you decide if Taltz is right for you.

IX CON BS 20AUG2024

ZEPBOUND INDICATIONS AND SAFETY SUMMARY WITH WARNINGS 
Zepbound® (ZEHP-bownd) is an injectable prescription medicine that may help adults with: 

• obesity, or some adults with overweight who also have weight-related medical problems to lose excess body weight and keep the weight off.
• moderate-to-severe obstructive sleep apnea (OSA) and obesity to improve their OSA. 

It should be used with a reduced-calorie diet and increased physical activity. 

Zepbound contains tirzepatide and should not be used with other tirzepatide-containing products or any GLP-1 receptor agonist medicines. It is not known if Zepbound is safe and effective for use in children. 

Warnings - Zepbound may cause tumors in the thyroid, including thyroid cancer. Watch for possible symptoms, such as a lump or swelling in the neck, hoarseness, trouble swallowing, or shortness of breath. If you have any of these symptoms, tell your healthcare provider. 

• Do not use Zepbound if you or any of your family have ever had a type of thyroid cancer called medullary thyroid carcinoma (MTC).
• Do not use Zepbound if you have Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).
• Do not use Zepbound if you have had a serious allergic reaction to tirzepatide or any of the ingredients in Zepbound. 

Zepbound may cause serious side effects, including: 
Severe stomach problems. Stomach problems, sometimes severe, have been reported in people who use Zepbound. Tell your healthcare provider if you have stomach problems that are severe or will not go away. 

Dehydration leading to kidney problems. Diarrhea, nausea, and vomiting may cause a loss of fluids (dehydration), which may cause kidney problems. It is important for you to drink fluids to help reduce your chance of dehydration. 

Gallbladder problems. Gallbladder problems have happened in some people who use Zepbound. Tell your healthcare provider right away if you get symptoms of gallbladder problems, which may include pain in your upper stomach (abdomen), fever, yellowing of skin or eyes (jaundice), or clay-colored stools. 

Inflammation of the pancreas (pancreatitis). Stop using Zepbound and call your healthcare provider right away if you have severe pain in your stomach area (abdomen) that will not go away, with or without vomiting. You may feel the pain from your abdomen to your back. 

Serious allergic reactions. Stop using Zepbound and get medical help right away if you have any symptoms of a serious allergic reaction, including swelling of your face, lips, tongue or throat, problems breathing or swallowing, severe rash or itching, fainting or feeling dizzy, or very rapid heartbeat. 

Low blood sugar (hypoglycemia). Your risk for getting low blood sugar may be higher if you use Zepbound with medicines that can cause low blood sugar, such as a sulfonylurea or insulin. Signs and symptoms of low blood sugar may include dizziness or light-headedness, sweating, confusion or drowsiness, headache, blurred vision, slurred speech, shakiness, fast heartbeat, anxiety, irritability, mood changes, hunger, weakness or feeling jittery. 

Changes in vision in patients with type 2 diabetes. Tell your healthcare provider if you have changes in vision during treatment with Zepbound. 

Depression or thoughts of suicide. You should pay attention to changes in your mood, behaviors, feelings or thoughts. Call your healthcare provider right away if you have any mental changes that are new, worse, or worry you. 

Food or liquid getting into the lungs during surgery or other procedures that use anesthesia or deep sleepiness (deep sedation). Zepbound may increase the chance of food getting into your lungs during surgery or other procedures. Tell all your healthcare providers that you are taking Zepbound before you are scheduled to have surgery or other procedures. 

Common side effects 
The most common side effects of Zepbound include nausea, diarrhea, vomiting, constipation, stomach (abdominal) pain, indigestion, injection site reactions, feeling tired, allergic reactions, belching, hair loss, and heartburn. These are not all the possible side effects of Zepbound. Talk to your healthcare provider about any side effect that bothers you or doesn't go away.

Tell your doctor if you have any side effects. You can report side effects at 1-800-FDA-1088 or www.fda.gov/medwatch. 

Before using Zepbound 

• Your healthcare provider should show you how to use Zepbound before you use it for the first time. 
• Talk to your healthcare provider about low blood sugar and how to manage it. Tell your healthcare provider if you are taking medicines to treat diabetes including an insulin or sulfonylurea.
• If you take birth control pills by mouth, talk to your healthcare provider before you use Zepbound. Birth control pills may not work as well while using Zepbound. Your healthcare provider may recommend another type of birth control for 4 weeks after you start Zepbound and for 4 weeks after each increase in your dose of Zepbound. 

Review these questions with your healthcare provider: 

• Do you have other medical conditions, including problems with your pancreas, or severe problems with your stomach, such as slowed emptying of your stomach (gastroparesis) or problems digesting food? 
• Do you take other diabetes medicines, such as insulin or sulfonylureas? 
• Do you have a history of diabetic retinopathy? 
• Are you scheduled to have surgery or other procedures that use anesthesia or deep sleepiness (deep sedation)? 
• Do you take any other prescription medicines or over-the-counter drugs, vitamins, or herbal supplements? 
• Are you pregnant, plan to become pregnant, breastfeeding, or plan to breastfeed? Zepbound may harm your unborn baby. Tell your healthcare provider if you become pregnant while using Zepbound. Zepbound may pass into your breast milk. You should talk with your healthcare provider about the best way to feed your baby while using Zepbound. 
• Pregnancy Exposure Registry: There will be a pregnancy exposure registry for women who have taken Zepbound during pregnancy. The purpose of this registry is to collect information about the health of you and your baby. Talk to your healthcare provider about how you can take part in this registry, or you may contact Lilly at 1-800-LillyRx (1-800-545-5979). 

How to take 

• Read the Instructions for Use that come with Zepbound.
• Use Zepbound exactly as your healthcare provider says. 
• Use Zepbound with a reduced-calorie diet and increased physical activity. 
• Inject Zepbound under the skin (subcutaneously) of your stomach (abdomen), thigh, or have another person inject in the back of the upper arm. Do not inject ZEPBOUND into a muscle (intramuscularly) or vein (intravenously).
• Use Zepbound 1 time each week, at any time of the day. 
• Change (rotate) your injection site with each weekly injection. Do not use the same site for each injection.
• If you take too much Zepbound, call your healthcare provider, call the Poison Help line at 1-800-222-1222 or go to the nearest hospital emergency room right away. 

Zepbound injection is approved as a 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, or 15 mg per 0.5 mL in single-dose pen or single-dose vial. 

Learn more 
Zepbound is a prescription medicine. For more information, call 1-800-LillyRx (1-800-545-5979) or go to www.zepbound.lilly.com. 

This summary provides basic information about Zepbound but does not include all information known about this medicine. Read the information that comes with your prescription each time your prescription is filled. This information does not take the place of talking with your healthcare provider. Be sure to talk to your healthcare provider about Zepbound and how to take it. Your healthcare provider is the best person to help you decide if Zepbound is right for you. 

ZP CON BS 25SEP2025 

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 

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. 

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 Taltz (ixekizumab) as a treatment for moderate to severe plaque psoriasis and active psoriatic arthritis and Zepbound (tirzepatide) as a treatment for adults with obesity or overweight, potential comprehensive treatment strategies for patients with moderate to severe plaque psoriasis and obesity, and the timeline for future readouts, 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 future study results will be consistent with the results to date, or that Lilly will execute its strategies as planned. For further discussion of these and other risks and uncertainties that could cause actual results to differ from Lilly's expectations, 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.

Refer to:	Kathleen Ritchie; kathleen.ritchie@lilly.com; 562-323-1667 (Lilly media)
	Michael Czapar; czapar_michael_c@lilly.com; 317-617-0983 (Investors)

 

 

View original content to download multimedia:https://www.prnewswire.com/news-releases/lillys-taltz-ixekizumab-and-zepbound-tirzepatide-used-together-delivered-superior-efficacy-in-first-of-its-kind-phase-3b-trial-for-adults-with-psoriasis-and-obesity-or-overweight-302691124.html

SOURCE Eli Lilly and Company

FAQ

What were the primary 36-week results of Lilly's TOGETHER-PsO trial (LLY)?

The primary endpoint was met: 27.1% reached PASI 100 plus ≥10% weight loss versus 5.8% on Taltz alone (p<0.001). According to the company, concomitant Taltz and Zepbound also met all key secondary endpoints at 36 weeks.

How did Taltz plus Zepbound perform on skin clearance (PASI 100) in the TOGETHER-PsO trial?

Taltz plus Zepbound achieved 40.6% PASI 100 versus 29.0% with Taltz alone (40% relative increase, p<0.05). According to the company, this demonstrates improved skin clearance when obesity is treated concurrently with Zepbound.

What safety signals were reported for combined Taltz and Zepbound in TOGETHER-PsO?

Adverse events were generally mild to moderate; common events included nausea, diarrhea, constipation, injection site reaction. According to the company, event types were consistent with each drug's known safety profile.

What patient population was enrolled in Lilly's TOGETHER-PsO study (LLY)?

The trial enrolled adults with moderate-to-severe plaque psoriasis and obesity/overweight with at least one weight-related comorbidity; mean BMI was >39 kg/m2. According to the company, many patients had extensive skin involvement and high-impact lesion locations.

Will Lilly (LLY) publish full TOGETHER-PsO 36-week data and discuss with regulators?

Yes. Detailed 36-week results will be published in a peer-reviewed journal and discussed with regulators. According to the company, full data will provide complete safety and efficacy context for the concomitant treatment approach.