> Trialight public data. Index of pages: https://trialight.com/llms.txt
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> Record changed: 2026-11-04

# A Study of Orforglipron in Participants With Overweight at Risk of Development of Obesity-Related Complications or Progression to Class 1 Obesity

NCT07794579

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

Phase

Phase 3

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

Recruitment status

Recruiting

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

Participants

2,001

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

Lead sponsor

Eli Lilly and Company

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

Start date

2026-08-26

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

Number of sites

180

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## Title and summary

**Summary**

This study will evaluate the efficacy and safety of orforglipron in participants with overweight and assess whether it helps reduce the future risk of obesity-related conditions, including type 2 diabetes, hypertension, and dyslipidemia, and progression to class 1 obesity.

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Acronym**

ATTAIN-NOW

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Short title**

A Study of Orforglipron in Participants With Overweight at Risk of Development of Obesity-Related Complications or Progression to Class 1 Obesity

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Official title**

A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Investigate the Efficacy and Safety of Once-Daily Oral Orforglipron Compared With Placebo in Individuals With Overweight at Risk of Development of Obesity-Related Complications or Progression to Class 1 Obesity

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## Status and phase

**Registry reports results**

No

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Listing at source**

Listed

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Recruitment status**

Recruiting

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Phase**

Phase 3

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Study type**

Interventional

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## Dates

**Completion date**

2030-09-01

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**First posted**

2026-08-31

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Registry last updated**

2026-10-08

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Primary completion date**

2029-08-01

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Start date**

2026-08-26

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## Size and sites

**Participants**

2,001

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Participant count basis**

Estimated

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Planned participants**

2,001

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Protocol amendments**

0

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Number of sites**

180

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## Sponsor and oversight

**Data monitoring committee**

No

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Registry sponsor category**

Industry

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Lead sponsor**

Eli Lilly and Company

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Source registry**

ClinicalTrials.gov

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## Identifiers

**Registry ID**

NCT07794579

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**ClinicalTrials.gov ID**

NCT07794579

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

**Registry record**

Open registry record

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## Study design

**Allocation**

Randomised

**Model**

Parallel groups

**Purpose**

Treatment

**Masking**

Double masking

**Masked roles**

Participants, Investigators

Sources for study design

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## Outcomes

### Primary outcomes

1. Time to Onset of Obesity Related Complications or Class 1 Obesity  
Timeframe: Baseline to Week 104  
Obesity related complications defined as type 2 diabetes, hypertension, or dyslipidemia; Class 1 obesity defined as body mass index (BMI) ≥30 kilograms per square meter (kg/m2) or an equivalent region-specific threshold

### Secondary outcomes

1. Percent Change from Baseline in Body Weight  
Timeframe: Baseline, Week 104
2. Time to Onset of Waist-to-Height Ratio ≥0.6  
Timeframe: Baseline to Week 104
3. Change from Baseline in Waist Circumference  
Timeframe: Baseline, Week 104
4. Time to Onset of Class 1 Obesity  
Timeframe: Baseline to Week 104
5. Time to First Occurrence of Composite Endpoint of Type 2 Diabetes, Hypertension, Dyslipidemia  
Timeframe: Baseline to Week 104
6. Time to Onset of Type 2 Diabetes  
Timeframe: Baseline to Week 104
7. Percent Change from Baseline in Total Fat Mass  
Timeframe: Baseline, Week 104
8. Change from Baseline in Systolic Blood Pressure  
Timeframe: Baseline, Week 104
9. Change from Baseline in Glycated Hemoglobin (HbA1c)  
Timeframe: Baseline, Week 104
10. Percent Change from Baseline in Triglycerides  
Timeframe: Baseline, Week 104
11. Change from Baseline in Impact of Weight on Quality of Life-Lite Clinical Trials Version (IWQOL-Lite-CT) Score  
Timeframe: Baseline, Week 104
12. Pharmacokinetics (PK): Steady-State Area Under the Curve (AUC) of Orforglipron  
Timeframe: Week 4, 12, 24, 52, and 76

Sources for outcomes

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## Eligibility

**Sex**

All

**Age groups**

Adults, Older adults

**Minimum age**

18 Years

**Healthy volunteers**

No

### Inclusion criteria

- Have an increased waist-to-height ratio of ≥0.5
- Have at least one pre-obesity-related complication (prediabetes, prehypertension, predyslipidemia)
- Have at least one unsuccessful attempt to reduce body weight based on diet and exercise
- Have a BMI greater than or equal to 25 to less than or equal to 29.9 kg/m2 or equivalent-/region-specific overweight thresholds

### Exclusion criteria

- Have type 1 diabetes, type 2 diabetes, or any other type of diabetes
- Do not have a stable body weight within 90 days before screening
- Have a documented obesity diagnosis or self-reported history of BMI ≥30 kg/m² (or an equivalent region-specific threshold)
- Have taken medications for weight loss, including over-the counter medications or alternative therapies, within 180 days prior to screening
- Have a prior or planned surgical treatment or procedure for obesity
- Have hypertension or history of hypertension
- Have dyslipidemia or history of dyslipidemia

Sources for eligibility

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## Sites

- Pinnacle Research Group, LLCAnniston, United StatesRecruiting
- Central Research AssociatesBirmingham, United StatesRecruiting
- Cahaba Research - PelhamPelham, United StatesRecruiting
- Care Access - 801 South Power Road, MesaMesa, United StatesRecruiting
- Absolute Clinical ResearchPhoenix, United StatesNot yet recruiting
- Synexus Clinical Research US, Inc./Orange Grove Family PracticeTucson, United StatesRecruiting
- Orange County Research CenterLake Forest, United StatesRecruiting
- Healthy Brain ClinicLong Beach, United StatesRecruiting
- Los Angeles Institute for Metabolic ResearchLos Angeles, United StatesRecruiting
- Desert Oasis Healthcare Medical GroupPalm Springs, United StatesRecruiting
- Artemis Institute for Clinical ResearchRiverside, United StatesRecruiting
- Riverside ClinicalRiverside, United StatesRecruiting
- Headlands Research- SacramentoSacramento, United StatesRecruiting
- Norcal Endocrinology & Internal MedicineSan Ramon, United StatesRecruiting
- Diablo Clinical Research, Inc.Walnut Creek, United StatesRecruiting
- Yale University School of MedicineNew Haven, United StatesNot yet recruiting
- Chase Medical Research, LLCWaterbury, United StatesRecruiting
- Excel Medical Clinical TrialsBoca Raton, United StatesRecruiting
- Flourish Research Acquisition, LLC dba Flourish Research - North MiamiMiami, United StatesRecruiting
- New Age Medical Research CorporationMiami, United StatesRecruiting
- Renstar Medical ResearchOcala, United StatesRecruiting
- Headlands Research OrlandoOrlando, United StatesRecruiting
- Oviedo Medical ResearchOviedo, United StatesRecruiting
- Care Access - St. PetersburgSt. Petersburg, United StatesRecruiting
- Precision Clinical ResearchSunrise, United StatesRecruiting

And 155 more, listed on the interactive page.

Sources for sites

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## References

- Related resource (trials.lilly.com)  
Source: [trials.lilly.com](https://trials.lilly.com/en-US/trial/736335)

### Other registry identifiers (2)

- 2026-526175-35-00
- J2A-MC-GZVA

Sources for references

Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07794579)

## Related records

### Drugs (1)

- [Orforglipron](https://trialight.com/data/asset/orforglipron-1138c12b-f1c7-45bb-b9ec-2b693f019a62.md)

### Lead sponsors (1)

- [Eli Lilly and Company](https://trialight.com/data/company/eli-lilly-and-company-9da7efcc-bafe-4b95-b30b-e87a97770db7.md)

### Conditions (2)

- [Prediabetes syndrome](https://trialight.com/data/condition/prediabetes-syndrome-c0783730-8a3c-56dc-9863-fded2cd8046c.md)
- [Vascular disorder](https://trialight.com/data/condition/vascular-disorder-024125e7-3020-5357-8a27-46e6e1b8178a.md)

### Targets (1)

- [GLP1R](https://trialight.com/data/target/glp1r-c31cc749-2d8a-54a9-9dab-84f5ee5d1742.md)

---

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