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CompletedNCT05295875Updated Nov 29, 2023

Efficacy and Safety of ALT-801 in the Treatment of Obesity

A Phase 2 interventional study of ALT-801 and Placebo in Obesity/Overweight, sponsored by Altimmune, Inc.. Completed at 31 sites in United States. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2023-11-29.

Sponsored by Altimmune, Inc. · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Primary completion was Sep 2023, 3 years ago, and no results have been posted to the registry.
Phase
Phase 2
Study type
Interventional
Enrollment
391
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This study will evaluate the efficacy and safety of ALT-801 once-weekly versus placebo as an adjunct to a reduced-calorie diet and increased physical activity in patients with obesity/overweight.

02

Conditions studied

  • Obesity/Overweight
03

In context

Obesity

6,297 studies on the registry are indexed under Obesity; 1,693 are open to participants now.

This study's enrollment of 391 is above the median of 78 across 4,879 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

Altimmune, Inc. is the lead sponsor of 19 studies on the registry; 1 is open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 4 (31%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Written informed consent signed prior to entry into the study
  • Male or female age 18 to 75 years, inclusive
  • Body mass index (BMI) ≥ 30 kg/m2 or BMI ≥ 27 kg/m2 combined with at least one obesity-related comorbidity
  • At least one unsuccessful weight loss attempt per investigator judgement
  • Agreement to comply with the study-required life-style intervention and treatment during the full duration of the study
  • Female subjects of childbearing potential who are not pregnant or breastfeeding, do not plan to become pregnant during the study, and agree to use effective birth control

Exclusion criteria

Exclusion Criteria:

  • Weight gain or loss > 5% in the 3 months prior to randomization or >10% in the 6 months prior to screening
  • Diabetes and related conditions:

    1. History or clinical evidence of diabetes mellitus of any type, including Type 1, Type 2, or mature onset diabetes of the young (MODY)
    2. HbA1c > 6.5%, fasting glucose ≥ 126 mg/dL (6.9 mmol/L), and/or random glucose of ≥ 200 mg/dL (11.0mmol/L) at screening
  • Obesity and related conditions:

    1. Obesity induced by known genetic causes or endocrine disorders (eg, Cushing Syndrome, inadequately treated hypothyroidism, defined as thyroid-stimulating hormone [TSH] > 6 mIU/L)
    2. History of bariatric surgery or other surgical treatment for obesity (eg, gastric banding, gastric bypass), or planned surgery or surgical treatment during the study. Liposuction and/or abdominoplasty performed >1 year before screening is allowed. Endoscopically placed intragastric balloons will be allowed if removed > 1 year before screening.
  • Gastrointestinal conditions:

    1. History of acute or chronic pancreatitis within 1 year (365 days) before screening
    2. History of or acute significant gastrointestinal (GI) disorder (eg, peptic ulcers, severe gastroesophageal reflux disease [GERD],
    3. History of GI surgery, including cholecystectomy and antrectomy. Surgery for appendicitis and small bowel resection >20cm is acceptable.
    4. History of inflammatory bowel disease, celiac disease or any medical condition or surgery that could affect gastric emptying, stool frequency or stool consistency. (Irritable bowel syndrome is permitted provided that bowel frequency and consistency are normal off treatment.)
  • Mental health conditions:

    1. Untreated depressive disorder, defined as a Patient Health Questionaire-9 (PHQ-9) score of ≥ 15 at screening
    2. Suicide ideation, defined as type 4 or 5 on the Columbia-Suicide Severity Rating Scale(C-SSRS) at screening, lifelong history of a suicide attempt, or suicidal behavior within 30 days before screening
    3. Other severe psychiatric disorder (eg, schizophrenia, bipolar disorder)
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
391 participants (actual)

Study arms

  • Experimental
    ALT-801 Dose Level 1

    Drug: ALT-801

  • Experimental
    ALT-801 Dose Level 2

    Drug: ALT-801

  • Experimental
    ALT-801 Dose Level 3

    Drug: ALT-801

  • Placebo comparator
    Placebo

    Other: Placebo

Interventions

  • DrugALT-801

    Injected subcutaneously (SC)

  • OtherPlacebo

    Injected subcutaneously (SC)

06

What researchers measure

Primary outcomes

  1. Relative change from baseline in body weight percentage

    Time frame: Baseline to Week 48

Secondary outcomes

  1. Percent proportion of subjects with weight loss of greater than or equal to 5%, 10%, and 15%

    Time frame: Baseline to Week 48

  2. Change from baseline in lipids

    Time frame: Baseline to Week 48

  3. The Number of Participants with One or More Treatment-Emergent Adverse Events (TEAEs)

    Time frame: Baseline to Week 48

  4. Changes from baseline in Fasting Glucose

    Time frame: Baseline to Week 48

  5. Changes from baseline in Hemoglobin A1c

    Time frame: Baseline to Week 48

  6. Changes from baseline in Homeostatic Marker Assessment for Insulin Resistance (HOMA-IR)

    Time frame: Baseline to Week 48

  7. Changes from baseline in: a) Systolic blood pressure, b) Diastolic blood pressure

    Time frame: Baseline to Week 48

  8. Change from baseline in proportion of patients using antihypertensive medications

    Time frame: Baseline to Week 48

07

Study locations

31 sites
  • Altimmune CTM
    Birmingham, Alabama 35020, United States
  • Altimmune CTM
    Mesa, Arizona 85201, United States
  • Altimmune CTM
    Los Angeles, California 90001, United States
  • National Research Institute
    Los Angeles, California 90057, United States
  • Altimmune CTM
    Montclair, California 91763, United States
  • Altimmune CTM
    Santa Barbara, California 93101, United States
  • Altimmune CTM
    Boca Raton, Florida 33427, United States
  • Altimmune CTM
    Clearwater, Florida 33755, United States
  • Altimmune CTM
    Fort Myers, Florida 33900, United States
  • Altimmune CTM
    Jacksonville, Florida 32201, United States
  • Altimmune CTM
    Port Orange, Florida 32123, United States
  • Altimmune CTM
    Sunrise, Florida 33319, United States
  • Altimmune CTM
    Savannah, Georgia 31411, United States
  • Altimmune CTM
    Evanston, Illinois 60201, United States
  • Altimmune CTM
    Indianapolis, Indiana 46201, United States
  • Midwest Institute for Clinical Research
    Indianapolis, Indiana 46260, United States
  • Altimmune CTM
    Louisville, Kentucky 40202, United States
  • Altimmune CTM
    Baton Rouge, Louisiana 70801, United States
  • Altimmune CTM
    New Orleans, Louisiana 70119, United States
  • Altimmune CTM
    Kansas City, Missouri 64101, United States
  • Altimmune CTM
    Butte, Montana 59701, United States
  • Altimmune CTM
    Berlin, New Jersey 08009, United States
  • Altimmune CTM
    New York, New York 10001, United States
  • Cornell University, Joan and Sanford Weill Medical College
    New York, New York 10065, United States
  • Altimmune CTM
    Cincinnati, Ohio 45201, United States
  • Altimmune CTM
    Philadelphia, Pennsylvania 19092, United States
  • Altimmune CTM
    Knoxville, Tennessee 37901, United States
  • Altimmune CTM
    Austin, Texas 78701, United States
  • Altimmune CTM
    Bellaire, Texas 77401, United States
  • Altimmune CTM
    San Antonio, Texas 78201, United States
  • Altimmune CTM
    Saint George, Utah 84770, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 29, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05295875
Lead sponsor
Altimmune, Inc.
Responsible party
Sponsor
First posted
Mar 25, 2022
Start date
Mar 31, 2022
Primary completion
Sep 28, 2023
Completion
Sep 28, 2023
Last update
Nov 29, 2023

Study contacts

Sarah K Browne, MD
study director · Altimmune, Inc.

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2023. You cannot join it, but the record below documents what was studied.

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