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Monoclonal Antibodies
LY3471851 for Healthy Subjects
Phase 1
Waitlist Available
Research Sponsored by Nektar Therapeutics
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up predose up to 56 days postdose
Awards & highlights
Study Summary
This study is evaluating whether a drug called LY3471851 can be safely administered under the skin.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ predose up to 56 days postdose
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~predose up to 56 days postdose
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
PK: Area Under the Concentration Versus Time Curve (AUC) of LY3471851
Pharmacokinetics (PK): Maximum Concentration (Cmax) of LY3471851
Side effects data
From 2023 Phase 2 trial • 291 Patients • NCT0443358516%
Injection site reaction
15%
Pyrexia
8%
Fatigue
7%
Nasopharyngitis
7%
Arthralgia
5%
Urinary tract infection
5%
Injection site erythema
5%
Injection site pain
5%
Alanine aminotransferase increased
5%
Anaemia
4%
COVID-19
4%
Bronchitis
4%
Injection site pruritus
4%
Asthenia
4%
Myalgia
4%
Pruritus
4%
Erythema
4%
Gamma-glutamyltransferase increased
3%
Pharyngitis
3%
Dyspepsia
3%
Pain in extremity
3%
Urticaria
3%
Rash
3%
Dermatitis contact
3%
Pityriasis rosea
3%
Influenza
3%
Pain
3%
Injection site rash
3%
Injection site swelling
3%
Nausea
3%
Back pain
3%
Headache
3%
Drug hypersensitivity
3%
Heavy menstrual bleeding
3%
Aspartate aminotransferase increased
1%
Vaccination complication
1%
Procedural pain
1%
Soft tissue injury
1%
Oedema peripheral
1%
Influenza like illness
1%
Swelling face
1%
Groin pain
1%
Limb injury
1%
Eosinophilia
1%
Iron deficiency anaemia
1%
Lymphadenitis
1%
Neutropenia
1%
Nasal obstruction
1%
Cough
1%
Nasal dryness
1%
Depression
1%
COVID-19 pneumonia
1%
Pyelonephritis
1%
Vomiting
1%
Chest pain
1%
Upper respiratory tract infection
1%
Furuncle
1%
Rhinitis
1%
Sinusitis
1%
Fungal infection
1%
Oral candidiasis
1%
Otitis externa
1%
Pharyngitis bacterial
1%
Viral infection
1%
Application site reaction
1%
Chills
1%
Feeling abnormal
1%
Injection site erosion
1%
Injection site exfoliation
1%
Injection site hypersensitivity
1%
Localised oedema
1%
Sensation of foreign body
1%
Diarrhoea
1%
Gastritis
1%
Dental caries
1%
Haemorrhoids
1%
Abdominal pain
1%
Mouth ulceration
1%
Oesophageal motility disorder
1%
Systemic lupus erythematosus
1%
Arthritis
1%
Neck pain
1%
Eczema
1%
Heart rate increased
1%
Urine protein/creatinine ratio increased
1%
Urinary sediment
1%
Dizziness
1%
Dysaesthesia
1%
Ophthalmic migraine
1%
Ligament sprain
1%
Joint dislocation
1%
Post procedural oedema
1%
Thermal burn
1%
Oropharyngeal pain
1%
Rhinorrhoea
1%
Hypotension
1%
Hot flush
1%
Delusion
1%
Seasonal allergy
1%
Myopia
1%
Dry eye
1%
Erythema of eyelid
1%
Vision blurred
1%
Bundle branch block right
1%
Vertigo
1%
Dysuria
1%
Pollakiuria
1%
Skin infection
1%
Rash maculo-papular
1%
Memory impairment
1%
Post procedural complication
1%
Hypertension
100%
80%
60%
40%
20%
0%
Study treatment Arm
LY3471851 High Dose
Placebo
LY3471851 Low Dose
LY3471851 Mid Dose
Trial Design
2Treatment groups
Experimental Treatment
Group I: LY3471851 (Thigh)Experimental Treatment1 Intervention
LY3471851 administered SC into the thigh.
Group II: LY3471851 (Abdomen)Experimental Treatment1 Intervention
LY3471851 administered subcutaneously (SC) into the abdomen.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
LY3471851
2021
Completed Phase 2
~670
Find a Location
Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
Nektar TherapeuticsLead Sponsor
58 Previous Clinical Trials
10,271 Total Patients Enrolled
Eli Lilly and CompanyIndustry Sponsor
2,619 Previous Clinical Trials
3,206,528 Total Patients Enrolled
Study DirectorEli Lilly and Company
1,347 Previous Clinical Trials
405,674 Total Patients Enrolled
Frequently Asked Questions
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