Inveltys

Chickenpox, Iritis, Inflammation + 10 more

Treatment

15 FDA approvals

20 Active Studies for Inveltys

What is Inveltys

Loteprednol

The Generic name of this drug

Alrex

is the brand name

image of different drug pills on a surface

Inveltys Overview & Background

Brand Name

Generic Name

First FDA Approval

How many FDA approvals?

Alrex

Loteprednol

1998

16

Approved as Treatment by the FDA

Loteprednol, otherwise called Alrex, is approved by the FDA for 15 uses like Ocular Inflammation and Inflammation .

Ocular Inflammation

Inflammation

Used to treat Inflammation in combination with Tobramycin

ocular bacterial infections

Used to treat ocular bacterial infections in combination with Tobramycin

Iritis

Inflammation

Used to treat Inflammation in combination with Tobramycin

Conjunctivitis infective

Seasonal Allergic Conjunctivitis

Conjunctivitis

Herpes Zoster Keratitis

Helps manage Herpes Zoster Keratitis

Inflammation

Used to treat Inflammation in combination with Tobramycin

Conjunctivitis

Iritis

Eye

Cyclitis

Superficial punctate keratitis

Helps manage Superficial punctate keratitis

When to interrupt dosage

The recommended measure of Inveltys is contingent upon the ascertained condition, including Ocular Inflammation, Conjunctivitis infective and Herpes Zoster Keratitis. The quantity of dosage shifts, as per the technique of delivery (e.g. Gel - Ophthalmic or Suspension/drops) noted in the table beneath.

Condition

Dosage

Administration

Inflammation

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Rosacea

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Conjunctivitis

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Conjunctivitis

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Cyclitis

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Eye

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Chickenpox

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Communicable Diseases

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Superficial punctate keratitis

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

ocular bacterial infections

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Iritis

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Seasonal Allergic Conjunctivitis

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Herpes Zoster Keratitis

, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %

Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment, Ointment - Ophthalmic, Suspension - Ophthalmic, Gel, Gel - Ophthalmic, Suspension

Warnings

Inveltys Contraindications

Condition

Risk Level

Notes

Keratitis, Dendritic

Do Not Combine

conjunctiva

Do Not Combine

Herpes Simplex

Do Not Combine

Chickenpox

Do Not Combine

Vaccinia

Do Not Combine

epithelial herpes simplex keratitis

Do Not Combine

Eye Infections, Fungal

Do Not Combine

Severe Hypersensitivity Reactions

Do Not Combine

Loteprednol may interact with Pulse Frequency

There are 20 known major drug interactions with Inveltys.

Common Inveltys Drug Interactions

Drug Name

Risk Level

Description

2,4-thiazolidinedione

Moderate

The risk or severity of hyperglycemia can be increased when Loteprednol is combined with 2,4-thiazolidinedione.

AICA ribonucleotide

Moderate

The risk or severity of hyperglycemia can be increased when Loteprednol is combined with AICA ribonucleotide.

AMG-222

Moderate

The risk or severity of hyperglycemia can be increased when Loteprednol is combined with AMG-222.

Acarbose

Moderate

The risk or severity of hyperglycemia can be increased when Loteprednol is combined with Acarbose.

Acetohexamide

Moderate

The risk or severity of hyperglycemia can be increased when Loteprednol is combined with Acetohexamide.

image of a doctor in a lab doing drug, clinical research

Inveltys Novel Uses: Which Conditions Have a Clinical Trial Featuring Inveltys?

198 active clinical trials are currently in progress to ascertain the efficacy of Inveltys in alleviating Seasonal Allergic Conjunctivitis, Iritis and Ocular Inflammation.

Condition

Clinical Trials

Trial Phases

Eye

0 Actively Recruiting

Conjunctivitis

0 Actively Recruiting

Communicable Diseases

0 Actively Recruiting

Superficial punctate keratitis

0 Actively Recruiting

Iritis

0 Actively Recruiting

Herpes Zoster Keratitis

0 Actively Recruiting

Rosacea

3 Actively Recruiting

Early Phase 1, Phase 2, Not Applicable

Conjunctivitis

0 Actively Recruiting

ocular bacterial infections

0 Actively Recruiting

Chickenpox

5 Actively Recruiting

Phase 4, Phase 3

Cyclitis

0 Actively Recruiting

Inflammation

61 Actively Recruiting

Not Applicable, Phase 2, Early Phase 1, Phase 3, Phase 1

Seasonal Allergic Conjunctivitis

0 Actively Recruiting

Inveltys Reviews: What are patients saying about Inveltys?

5

Patient Review

2/7/2020

Inveltys for Inflammation of the Eye Following Surgery

I've been using these eye drops for months, first for post-surgery and later for my dry eye. Applying them twice daily really helped with the swelling and vision. I also found that I didn't have to rub my eyes as much when using inveltys which was a huge plus.

4.3

Patient Review

8/2/2021

Inveltys for Inflammation of the Eye Following Surgery

I'm a few weeks out from surgery and my eyes feel much more relaxed. I tried another product previously that was in gel form, but it felt really uncomfortable. This one works better for me. It's a little pricy, but it's worth trying.

2.3

Patient Review

8/29/2022

Inveltys for Inflammation of the Eye Following Surgery

I wasn't a fan of this bottle. It wasted a lot of product and was difficult to use.

2

Patient Review

5/9/2019

Inveltys for Inflammation of the Eye Following Surgery

surgery was two weeks ago and my eyes are still swollen. Not only that, but my vision has become cloudy. I don't see the appeal of this drug at all.

2

Patient Review

5/17/2020

Inveltys for Inflammation of the Eye Following Surgery

I'm using this medication for the inflammation of my retina following cataract surgery, but I have yet to see any improvement. It's a very expensive drug with little to show for it so far.
image of drug pills surrounding a glass of water symbolizing drug consumption

Patient Q&A Section about inveltys

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is another name for Inveltys?

"Only for ophthalmic use.

Inveltys is an eye drop that contains a steroid. It is used to treat inflammation."

Answered by AI

What are the side effects of Inveltys eye drops?

"The following are symptoms of eye allergies: headaches, burning, eye irritation, itching, dry eyes, blurred eyesight, feeling that something is in the eye, runny nose."

Answered by AI

How long should you use Inveltys after cataract surgery?

"Apply one or two drops of the solution into the affected eye up to four times a day, starting 24 hours after the surgery was performed. Continue using the solution for two weeks."

Answered by AI

What does Inveltys do for the eye?

"Inveltys is a steroid eye drop used to treat inflammation caused by allergies, shingles, severe acne, iritis, or other conditions. It can also help relieve pain and swelling after eye surgery."

Answered by AI

Clinical Trials for Inveltys

Image of Texas Tech University Health Sciences Center/ University Medical Center Lubbock in Lubbock, United States.

PSP Monitoring for Sepsis in Burns

18 - 89
All Sexes
Lubbock, TX

The goal of this clinical trial is to learn if using pancreatic stone protein (PSP) test results helps doctors find and treat sepsis earlier in adults with serious burn injuries. The study will also look at whether using PSP is safe and practical in the burn intensive care unit. The main questions it aims to answer are: * Does seeing PSP test results help doctors start the right antibiotics sooner? * Does using PSP reduce unnecessary antibiotic use? * Does using PSP improve recovery and other health outcomes? Researchers will compare two groups of patients. One group will receive standard care, and their PSP test results will be hidden from their care team. The other group will receive standard care, but their care team will be able to see the PSP test results and use them to help make treatment decisions. Participants will: * Be randomly assigned to one of the two study groups. * Have a small blood sample taken within 24 hours after being admitted to the burn ICU and then once each weekday while they are in the ICU. * Receive the usual care for burn injuries and sepsis throughout the study.

Waitlist Available
Has No Placebo

Texas Tech University Health Sciences Center/ University Medical Center Lubbock

Brian Schneider, MD

Abionic SA

Image of Nicholas Institute of Sports Medicine & Athletic Trauma (NISMAT) in New York, United States.

Fruit Juice for Inflammation

18 - 65
All Sexes
New York, NY

Dietary patterns and physical inactivity common in Western societies have been associated with chronic low-grade inflammation and an increased risk of non-communicable health conditions. Fruits and vegetables contain polyphenols and other bioactive compounds that may have antioxidant and anti-inflammatory properties and may influence inflammatory biomarkers. This study will evaluate the effects of increased consumption of a fruit juice on inflammatory biomarkers and exercise capacity in adults with mildly elevated inflammation. Approximately 40 participants will be randomly assigned to consume one of two fruit juice interventions daily for approximately 2 weeks. Changes in C-reactive protein (CRP) and exercise capacity, assessed using a 6-minute walk test, will be evaluated before and after the intervention and compared between the two groups.

Recruiting
Has No Placebo

Nicholas Institute of Sports Medicine & Athletic Trauma (NISMAT)

Christopher Tanayan, MD

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Image of Children's Clinic of Jonesboro, AR in Jonesboro, United States.

MMRV Vaccines for Measles, Mumps, Rubella, and Chickenpox

4 - 6
All Sexes
Jonesboro, AR

The purpose of this study is to evaluate how consistently 3 different manufacturing lots of the GSK's investigational measles, mumps, rubella, and varicella (MMRVNS) vaccine will produce an immune response. It will also compare the overall immune response to the MMRVNS vaccine with that of the Merck licensed measles, mumps, rubella, and varicella (MMRV) vaccine. The vaccines will be given as a second dose to children aged 4 to 6 years who have previously received a first dose of any combination of measles, mumps, rubella, and varicella-containing vaccine(s). The study will also assess the immune response and safety of the MMRVNS and MMRV vaccines when given at the same time as a diphtheria, tetanus, acellular pertussis, and inactivated poliovirus (DTaP-IPV) vaccine. The DTaP-IPV vaccine used is licensed as Kinrix in the United States.

Phase 3
Waitlist Available

Children's Clinic of Jonesboro, AR (+35 Sites)

GlaxoSmithKline

Image of University of Utah in Salt Lake City, United States.

Metformin for Muscle Weakness

18+
All Sexes
Salt Lake City, UT

The purpose of this research study is to determine if Metformin taken after anterior cruciate ligament reconstruction (ACLR) surgery can decrease muscle fibrosis, cellular senescence and improve leg strength. ACL injury and surgery increase muscle collagen content and inflammation which slows the recovery of muscle and function and ultimately impacts the quality of life. Individuals enrolled in the study will be randomized to receive metformin (or placebo) for 4 months after surgery. The investigators will measure muscle strength and inflammatory markers in muscle biopsy samples after the intervention period. Investigators will also follow up with participants 8 months later to determine the lasting effects of the intervention.

Phase < 1
Waitlist Available

University of Utah

Micah Drummond

Image of Reichwald Health Sciences Centre in Kelowna, Canada.

Broccoli Sprout Extract + Exercise for Inflammation

19 - 35
All Sexes
Kelowna, Canada

The study consist of 3 interventional periods which will be completed by each consenting participant in a randomized, crossover fashion. The interventional periods will be separated by a minimum 1 week washout period. One of the interventions consists of 4 days of daily supplementation with the commercially available broccoli sprout extract capsules (BrocElite). Another intervention will consist of 4 days of daily supervised treadmill running. The exercise protocol consists of 4 minutes of high-intensity running running followed by a 3 minute recovery period, repeated for a total of 4 repetitions. The last intervention combines the above two and consists of 4 days of daily supplementation and daily supervised exercise training. Before and after each intervention, basic anthropometrics (weight, heart rate, and blood pressure) will be recorded, and a venous blood sample will be collected. Blood samples will be analyzed for metabolic and inflammatory markers. Participants will be asked to refrain from structured exercise, alcohol consumption, and broccoli consumption during each of the experimental periods. Before any testing, willing participants will provide informed consent, and fill out a few demographic, and lifestyle questionnaires. The study will be conducted at the University of British Columbia in Kelowna, BC, Canada.

Recruiting
Has No Placebo

Reichwald Health Sciences Centre

Image of Vanderbilt University Medical Center in Nashville, United States.

2-HOBA for Salt Sensitivity of Blood Pressure

18+
All Sexes
Nashville, TN

Hypertension is the leading cause of preventable deaths globally, driven by complications such as myocardial infarction, stroke, heart failure, and kidney disease. Recent updates in hypertension classification by the American Heart Association (AHA) place nearly half of the U.S. population in the hypertensive category. Excess dietary salt is a major risk factor for hypertension, with 50% of hypertensive individuals exhibiting salt-sensitivity of blood pressure (SSBP). SSBP is an independent predictor of cardiovascular events and death. While kidney mechanisms in salt-sensing have been extensively studied, emerging evidence suggests that immune cells can also sense sodium (Na+). This trial hypothesizes that myeloid cell-derived isolevuglandins (IsoLGs) drive endothelial dysfunction, perpetuating the salt-sensitive phenotype. Preliminary data indicate that targeting IsoLGs with the IsoLG scavenger 2-hydroxybenzylamine (2-HOBA) may interrupt this immune-vascular axis, reducing salt sensitivity and associated cardiovascular risks. This phase 2 clinical trial aims to investigate the role of 2-HOBA in modulating immune cell function within blood vessels in hypertensive patients. The study will explore the impact of immunity on salt sensitivity and assess 2-HOBA's potential to reduce endothelial dysfunction, improve immune cell activation, and alleviate SSBP.

Phase 2
Waitlist Available

Vanderbilt University Medical Center

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Image of University of Oklahoma Health Campus in Oklahoma City, United States.

Disulfiram for Rheumatoid Arthritis

18 - 75
All Sexes
Oklahoma City, OK

Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by persistent joint inflammation and systemic immune activation. Obesity is common among individuals with RA and is associated with increased disease activity, reduced treatment response, and worse functional outcomes. Inflammation in adipose tissue, driven in part by activation of the NLRP3 inflammasome and downstream gasdermin D (GSDMD)-mediated pathways, may contribute to systemic inflammation and RA disease severity. Disulfiram (DSF), an FDA-approved medication for alcohol use disorder, has recently been identified as an inhibitor of GSDMD-mediated inflammatory signaling and pyroptosis. Preclinical studies suggest that DSF reduces inflammasome activation, inflammatory cytokine release, and metabolic dysfunction. This study is a 12-week, randomized, double-blind, placebo-controlled pilot trial designed to evaluate the safety, tolerability, and preliminary efficacy of DSF in overweight and obese adults with active RA despite stable disease-modifying antirheumatic drug (DMARD) therapy. Participants will be randomized to receive either DSF (250 mg daily) or placebo. The primary objective is to assess safety and tolerability. Secondary and exploratory objectives include evaluating the effects of DSF on systemic inflammation, RA disease activity, metabolic parameters, and adipose tissue inflammasome activation. Findings from this study will inform the feasibility and design of larger clinical trials targeting GSDMD-mediated inflammation in RA.

Phase 2
Waitlist Available

University of Oklahoma Health Campus

Beatriz Y Hanaoka, MD, MSc

Image of University of California, Riverside in Riverside, United States.

Acetazolamide for Altitude Sickness

18 - 65
All Sexes
Riverside, CA

High altitude travel can lead to inflammation in the body and activation of innate immune cells. The investigators' prior research demonstrates that 1 to 3 days at 3800 m elevation leads to increased expression of genes in blood cells that code for proteins that signal cell damage (damage associated molecular patterns (DAMPs)), cell receptors involved in innate immune responses, as well as increases in monocyte and neutrophil cells which promote inflammation. This study will investigate the potential mechanisms underlying these effects using the drug Acetazolamide, a carbonic anhydrase inhibitor which is known to reduce symptoms of Acute Mountain Sickness.

Phase < 1
Waitlist Available

University of California, Riverside

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We made a collection of clinical trials featuring Inveltys, we think they might fit your search criteria.
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