Inveltys

Chickenpox, Iritis, Inflammation + 10 more
Treatment
14 FDA approvals
20 Active Studies for Inveltys

What is Inveltys

LoteprednolThe Generic name of this drug
Alrexis 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 14 uses like Ocular Inflammation and ocular bacterial infections .
Ocular Inflammation
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 - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
Rosacea
, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %
Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
Conjunctivitis
, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %
Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
Conjunctivitis
, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %
Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
Cyclitis
, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %
Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
Eye
, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %
Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
Chickenpox
, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %
Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
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 - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
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 - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
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 - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
Iritis
, 2.0 mg/mL, 0.005 mg/mg, 5.0 mg/mL, 0.2 %, 0.5 %
Ophthalmic, Suspension / drops, Suspension / drops - Ophthalmic, , Ointment - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
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 - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic
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 - Ophthalmic, Ointment, Suspension - Ophthalmic, Suspension, Gel, Gel - Ophthalmic

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.
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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
2 Actively Recruiting
Early Phase 1, Phase 2
Conjunctivitis
0 Actively Recruiting
ocular bacterial infections
0 Actively Recruiting
Chickenpox
4 Actively Recruiting
Phase 4, Phase 3
Cyclitis
0 Actively Recruiting
Inflammation
58 Actively Recruiting
Not Applicable, Early Phase 1, Phase 1, Phase 2, Phase 3, Phase 4
Seasonal Allergic Conjunctivitis
0 Actively Recruiting

Inveltys Reviews: What are patients saying about Inveltys?

5Patient 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.
4.3Patient 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.
2.3Patient 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.
2Patient 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.
2Patient 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.
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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 UConn Health in Farmington, United States.

Cognitive Remediation for Memory and Thinking Difficulties

18+
All Sexes
Farmington, CT
The goal of this clinical trial is to determine if a neuroscience-based computerized cognitive remediation ("brain training") program can treat neurocognitive dysfunction (i.e., memory or thinking difficulties) that emerges in some older adults following a viral infection. The main questions it aims to answer are: * Does computerized cognitive remediation improve cognitive performance and day-to-day functioning in older adults with postviral neurocognitive dysfunction? * Will treatment effects be maintained over time, leading to better long term cognitive outcomes? * Does the treatment lead to reductions in blood-based markers of inflammation as a potential mechanism of cognitive symptom improvement? * Can the treatment be optimized and refined based on feedback from participants to improve user (patient) experience? Researchers will compare the computerized cognitive remediation program to an active computer-based control condition (alternative computer activities) to see if the computerized cognitive remediation program works to treat postviral neurocognitive dysfunction. Participation takes approximately 43-48 hours over 7 months, with most activities (40-46 hours) completed within the first 7-8 weeks, including: * Initial intake visit: Eligibility confirmation (\~2-3 hours) * Computer activities: About 5 hours per week for \~6 weeks (total \~30 hours) completed on a computer tablet provided by the study and loaned to participants for use during the treatment phase * Weekly remote check-in meetings: \~30 minutes each during treatment * Blood draws: Two sessions (before and after treatment), \~20-30 minutes each * Three research visits: Pre-treatment, post-treatment, and 6-month follow-up (\~2-3 hours each, including assessments of cognitive, emotional, and daily functioning)
Waitlist Available
Has No Placebo
UConn HealthCutter Lindbergh, Ph.D.
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Freeze-dried Grape Powder for Healthy Aging

50 - 75
All Sexes
Storrs, CT
The purpose of this study is to investigate the effects of consuming grape powder on immune profiles in healthy middle- and older-aged individuals. Specifically, the investigators are interested in evaluating the potential effects of grapes in influencing markers of immune function, inflammation, and metabolism that are known to change with aging. Grapes contain several nutrients and antioxidant polyphenols such as resveratrol, quercetin, vitamin K and fiber, which are known to promote heart and immune health. However, the effects of grapes on altering immune profiles within the context of aging is not well understood. Therefore, this study will explore how daily grape consumption impacts certain markers of immunity in healthy middle- and older-aged adults. The main study procedures include consumption of a freeze-dried grape powder and control powder (which tastes the same but has none of the grape compounds that are being studied) mixed with water as a beverage on a daily basis for 4 weeks each. The investigators will additionally ask that participants avoid eating grapes and certain other antioxidant/grape-related foods and beverages throughout the 13-week study. Participants will additionally be asked to complete surveys about their diet, physical activity, and medical history, as well as provide blood samples and body weight measures throughout the course of the study. Participation in the study is expected to last about 6.25 hours over the course of 13 weeks and will include 7 visits.
Recruiting
Paid Trial
Department of Nutritional Sciences
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Orticumab for Heart Attack

18+
All Sexes
Los Angeles, CA
The goal of this clinical trial is to determine the clinical effect of orticumab treatment on inflammation in study participants with prior myocardial infarction who have elevated coronary inflammation based on CCTA. The main question it aims to answer is: Clinical effects of orticumab treatment on inflammation of the coronary artery parameters measured with CCTA Researchers will compare the effects with placebo group after 6 months of treatment Participants will Keep the planned study visit appointments Provide complete information about medical and medical history Speak to the study doctor before changing any of non-study treatments, including starting new medications, receiving any vaccinations, or setting out to join any other clinical studies
Phase 2
Recruiting
Abcentra Investigational Site (+6 Sites)Abcentra
Have you considered Inveltys clinical trials? We made a collection of clinical trials featuring Inveltys, we think they might fit your search criteria.Go to Trials
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Biophoton Therapy for Stem Cell Proliferation

18 - 70
All Sexes
Tampa, FL
Study Objective The purpose of this clinical study is to evaluate if biophoton therapy, delivered by Tesla BioHealing® Biophoton Generators (Biophotonizer), can increase self-grown stem cells naturally. Study Design This is a randomized, double-blinded, placebo-controlled intervention clinical study to assess the effectiveness of biophoton therapy in impacting stem cells. Approximately 46 volunteers who want to increase self-grown stem cells will participate in the study. Study Randomization The biostatistician will prepare a randomization schedule including a serial of subject numbers. A subject number will be randomly assigned to each study participant, which will assign them to either the control group or the treatment group. Other than the Informed Consent Form (ICF), all study information will be recorded by using the subject number. The Principal Investigator, study physicians, study nurse, data-entry specialists, and biostatisticians, as well as the participants, will be blinded about who received which product during the first two weeks of study participation.
Recruiting
Online Trial
Tesla MedBed at Tampa-FL (+1 Sites)James Z Liu, MD, PhD
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Physical Activity for Delayed Onset Muscle Soreness

18 - 35
All Sexes
Toronto, Canada
After completing novel activity or exercise we may experience exercise-induced muscle damage (EIMD), resulting in a period of reduced muscle function and delayed onset muscle soreness (DOMS). DOMS is characterized by muscle pain and tenderness that typically resolves within a week. While the precise cause of DOMS is unknown, there is growing evidence implicating damage to the connective tissue that surrounds our muscle fibers and is related to a small amount of inflammation. This inflammation is a normal part of our body's ability to recovery from injuries and may be visualized through the use of ultrasound technology. A variety of recovery techniques have been proposed that may help with the recovery of DOMS such as massage and electrical muscle stimulation, but these are not always accessible. Therefore, we are interested in investigating whether the number of daily steps can affect how you experience DOMS.
Waitlist Available
Has No Placebo
Goldring Center for High Performance Sport
Have you considered Inveltys clinical trials? We made a collection of clinical trials featuring Inveltys, we think they might fit your search criteria.Go to Trials
Have you considered Inveltys clinical trials? We made a collection of clinical trials featuring Inveltys, we think they might fit your search criteria.Go to Trials
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