Pred Forte

Inflammation, Conjunctivitis, Conjunctivitis + 4 more

Treatment

4 FDA approvals

20 Active Studies for Pred Forte

What is Pred Forte

Prednisolone acetate

The Generic name of this drug

Treatment Summary

Prednisolone acetate is a medication used to treat inflammation and other related conditions. It contains prednisolone, a steroid, combined with an acetate group. Prednisolone acetate was approved by the FDA in 1955.

Blephamide

is the brand name

image of different drug pills on a surface

Pred Forte Overview & Background

Brand Name

Generic Name

First FDA Approval

How many FDA approvals?

Blephamide

Prednisolone acetate

1961

39

Approved as Treatment by the FDA

Prednisolone acetate, also known as Blephamide, is approved by the FDA for 4 uses including Inflammation and Organ Transplantation .

Inflammation

Organ Transplantation

Inflammation

Inflammatory Conditions

Helps manage Inflammatory Conditions

Effectiveness

How Pred Forte Affects Patients

Prednisolone acetate is a type of corticosteroid drug that blocks the body's pro-inflammatory signals and encourages anti-inflammatory signals. Its effects wear off quickly, with a half life of 2-3 hours. Corticosteroids can be taken in doses much higher than the body's natural production, and this has a wide therapeutic window. Taking corticosteroids can have side effects such as suppression of the hypothalamic-pituitary-adrenal axis and increased risk of infections, so patients should be aware of these risks.

How Pred Forte works in the body

Corticosteroids reduce swelling and stop white blood cells from flowing to sites of inflammation. This is done by changing the expression of certain genes. Corticosteroids also prevent cells from dying and stop the formation of chemicals that cause inflammation. Lower doses of corticosteroids help with inflammation, while higher doses weaken your immune system. Very high doses of corticosteroids can cause too much sodium and too little potassium in the body.

When to interrupt dosage

The advised measure of Pred Forte is contingent upon the identified disorder, including Ocular Infections, Irritations and Inflammations, Ocular Inflammation and Inflammatory Conditions. The sum of dosage differs, according to the technique of delivery (e.g. Ophthalmic or Solution / drops - Ophthalmic) featured in the table below.

Condition

Dosage

Administration

Conjunctivitis

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops, Suspension / drops - Ophthalmic, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ointment - Ophthalmic; Topical, Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit - Ophthalmic, Kit

Conjunctivitis

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops, Suspension / drops - Ophthalmic, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ointment - Ophthalmic; Topical, Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit - Ophthalmic, Kit

Ocular Infections, Irritations and Inflammations

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops, Suspension / drops - Ophthalmic, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ointment - Ophthalmic; Topical, Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit - Ophthalmic, Kit

Organ Transplantation

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops, Suspension / drops - Ophthalmic, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ointment - Ophthalmic; Topical, Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit - Ophthalmic, Kit

Eye Infections, Bacterial

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops, Suspension / drops - Ophthalmic, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ointment - Ophthalmic; Topical, Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit - Ophthalmic, Kit

Inflammation

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops, Suspension / drops - Ophthalmic, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ointment - Ophthalmic; Topical, Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit - Ophthalmic, Kit

Inflammatory Conditions

0.002 mg/mg, , 10.0 mg, 10.0 mg/mL, 2.0 mg/mL, 1.2 mg/mL, 0.2 %, 1.0 %, 0.12 %, 0.006 mg/mg, 0.5 %, 1.25 mg/mL, 1.0 mg/mL, 10.0 mg/mg, 1.25 mg, 5.0 mg/mL, 16.7 mg/mL, 0.005 mg/mg

, Ointment, Ophthalmic, Ointment - Ophthalmic, Oral, Suspension, Suspension - Oral, Suspension / drops, Suspension / drops - Ophthalmic, Suspension - Ophthalmic, Solution / drops, Solution / drops - Ophthalmic, Ointment - Ophthalmic; Topical, Ophthalmic; Topical, Solution, Solution - Ophthalmic, Kit - Ophthalmic, Kit

Warnings

Pred Forte has one contraindication and should not be ingested if you are suffering from any of the conditions detailed in the following table.

Pred Forte Contraindications

Condition

Risk Level

Notes

Severe Hypersensitivity Reactions

Do Not Combine

Prednisolone Acetate may interact with Pulse Frequency

There are 20 known major drug interactions with Pred Forte.

Common Pred Forte Drug Interactions

Drug Name

Risk Level

Description

Abemaciclib

Major

The metabolism of Abemaciclib can be increased when combined with Prednisolone acetate.

Acalabrutinib

Major

The metabolism of Acalabrutinib can be increased when combined with Prednisolone acetate.

Alectinib

Major

The metabolism of Alectinib can be increased when combined with Prednisolone acetate.

Alpelisib

Major

The metabolism of Alpelisib can be increased when combined with Prednisolone acetate.

Aminophylline

Major

The metabolism of Aminophylline can be increased when combined with Prednisolone acetate.

Pred Forte Toxicity & Overdose Risk

The lowest toxic dose of prednisolone acetate in mice is 1680mg/kg. People who overdose on this drug may experience more severe side effects of corticosteroids. If the overdose occurred recently, treatment may include stomach pumping or inducing vomiting. For long-term overdose, doctors may reduce the dose or have patients take the drug every other day. An overdose through the eyes is not likely to cause problems.

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

Pred Forte Novel Uses: Which Conditions Have a Clinical Trial Featuring Pred Forte?

At present, 189 active trials are exploring the potential of Pred Forte in alleviating Inflammation, Inflammatory Conditions and Superficial Ocular Infections.

Condition

Clinical Trials

Trial Phases

Inflammation

57 Actively Recruiting

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

Conjunctivitis

0 Actively Recruiting

Eye Infections, Bacterial

0 Actively Recruiting

Ocular Infections, Irritations and Inflammations

0 Actively Recruiting

Conjunctivitis

0 Actively Recruiting

Organ Transplantation

0 Actively Recruiting

Inflammatory Conditions

1 Actively Recruiting

Phase 2

Pred Forte Reviews: What are patients saying about Pred Forte?

5

Patient Review

7/22/2012

Pred Forte for Inflammation of the Eye

I've been on this medication for a few weeks now, three times a day. I'm sure it's effective, but the taste is absolutely vile. It lingers in your mouth for hours afterwards and makes my stomach hurt. I'll be calling the doctor on Monday morning to discuss other options.

5

Patient Review

2/6/2012

Pred Forte for Inflammation of the Iris and Ciliary Body of the Eye

I've been using this product for 24 years to treat iritis. In my experience, it stings and burns like acid. Be prepared for the pain if you decide to use this treatment.

5

Patient Review

6/29/2022

Pred Forte for Inflammation of the Iris - the Colored Part of the Eyeball

These drops have saved my eyeballs on two separate occasions! They caused a slight increase in eye pressure but it was still within the limit. I took them like a champion and my eyes love them!

5

Patient Review

7/17/2016

Pred Forte for Inflammation of the Iris and Ciliary Body of the Eye

I would recommend you consider all potential risks before taking this medication. It did help with the inflammation, but caused an infection that has now led to surgery being required to fix my lazy eye.

4.7

Patient Review

1/9/2022

Pred Forte for Inflammation of the Eye

I used Pred Forte Eyedrops for a week after some perfume got in my eye and caused inflammation. I gradually stopped using it as per the doctor's direction, and for 2 days it was good. But then the inflammation came back. Now I have to use this over a month, gradually reducing the number of times I use it each day. Make sure you use some drops like Refresh Tears along with it to avoid burning/ irritation.

4.3

Patient Review

2/28/2011

Pred Forte for Inflammation of the Eye Following Surgery

4

Patient Review

3/28/2012

Pred Forte for Inflammation of the Eye Following Surgery

I had cornea transplants in both eyes and have been taking this six times a day as prescribed. Unfortunately, I've experienced several negative side effects like swelling of the face and eyes, vomiting, and blurred vision. I'm also now suffering from much worse allergies than before. I've brought this up to my doctors but they don't believe me.

4

Patient Review

12/15/2011

Pred Forte for Severe Inflammation of the Eye

I was prescribed this after having PRK Lasik. I had terrible reactions to this medication, feeling depressed, high heart rate and major anxiety. I asked to be taken off of it right away!

4

Patient Review

4/13/2021

Pred Forte for Inflammation of the Iris and Ciliary Body of the Eye

I've been using these drops for a few weeks now and I'm starting to feel like I might be too dependent on them. My vision has become quite blurry, to the point where I have difficulty seeing screens. However, it has been effective in reducing pain and inflammation.

3.3

Patient Review

2/18/2013

Pred Forte for Inflammation of the Eye Following Surgery

I had PRK surgery and started taking this medication. However, I began to feel dizzy each day, so I stopped after a week even though the doctor wanted me to take it for a month. If you experience side effects like this, listen to your body and stop taking the medication immediately.

3

Patient Review

5/12/2014

Pred Forte for Inflammation of the Eye

I developed some eye problems and impotence after just three months of using this treatment.

2.7

Patient Review

6/23/2013

Pred Forte for Severe Inflammation of the Eye

After a month of taking this drug following a glaucoma operation, my anxiety has flared up from time to time. I'm not sure if it's the medication or if it's residual trauma from the pain of glaucoma, but I trust my doctors and will continue to take it as directed.

2.3

Patient Review

9/28/2020

Pred Forte for Inflammation of the Eye Following Surgery

Following Lasik, I used this treatment to target epithelial cells. It did the job, but came with a whole host of terrible side effects: anxiety, depression, feeling pressure in my face, and exhaustion.

2.3

Patient Review

5/11/2012

Pred Forte for Inflammation of the Eye Following Surgery

I've found that my blood sugar has increased since I began using this medication.

1.7

Patient Review

4/27/2011

Pred Forte for Inflammation of the Eye Following Surgery

image of drug pills surrounding a glass of water symbolizing drug consumption

Patient Q&A Section about pred forte

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

How long should I use Pred Forte?

"Use eye drops for no longer than one week unless directed by a doctor. Prolonged use can cause issues within your eye."

Answered by AI

Is Pred Forte a steroid?

"Prednisolone, brand name Pred Forte, is a steroid medication used to treat eye conditions characterized by inflammation or sensitivity to light. It is effective in controlling allergic reactions and reducing swelling."

Answered by AI

What are the side effects of Pred Forte eye drops?

"Using this medication may cause burning, stinging, or itching in the eyes for 1-2 minutes. You may also have temporary cloudy vision, increased sensitivity to light, or visual disturbances such as blurry vision. Some people feel like there is something in their eye after using this medication. Allergic reactions are also a possible side effect."

Answered by AI

What is Pred Forte used for?

"PRED FORTE is used to treat eye inflammation in adults. Short-term use of this medication can help to reduce the burning, redness, swelling, and irritation that is associated with inflammation of the eye caused by chemicals, heat, radiation, allergies, or foreign objects."

Answered by AI

Clinical Trials for Pred Forte

Image of Exercise and Performance Nutrition Laboratory in Saint Charles, United States.

Multi-Strain Postbiotic for Inflammation and Gastrointestinal Symptoms

18 - 55
All Sexes
Saint Charles, MO

This study will evaluate the effects of a multi-strain postbiotic supplement on markers of inflammation, immune function, gastrointestinal symptoms, psychological well-being, and intestinal permeability in healthy adults. The primary objective is to determine whether four weeks of postbiotic supplementation alters physiological and perceptual responses to a standardized bout of moderate-to-high intensity exercise compared with placebo. Approximately 50 healthy men and women aged 18 to 55 years will be enrolled in a randomized, double-blind, placebo-controlled, parallel-group clinical trial. Participants will be randomly assigned to receive either a multi-strain postbiotic supplement or a matched placebo for 28 days. At the end of the supplementation period, participants will complete a 45-minute treadmill exercise bout at 75% of their individually determined maximum heart rate. Blood samples will be collected to assess biomarkers of inflammation, immune activity, and recovery. Gastrointestinal symptoms, intestinal permeability, anxiety, and perceived recovery will be evaluated using validated questionnaires. This study is designed to determine whether postbiotic supplementation modulates physiological stress responses and subjective well-being following prolonged exercise in healthy adults.

Waitlist Available
Paid Trial

Exercise and Performance Nutrition Laboratory

Chad M Kerksick, PhD

Image of ATX Hyperbarics in Austin, United States.

Hyperbaric Oxygen Therapy for Cardiovascular Fitness

30 - 60
All Sexes
Austin, TX

The purpose of this study is to determine whether hyperbaric oxygen therapy (HBOT) at 1.75 atmospheres of pressure (ATA) improves cardiovascular fitness (VO₂ max) and reduces inflammation in healthy adults. HBOT involves breathing pure oxygen in a pressurized chamber and is considered investigational for this use. Recent research has shown that different HBOT pressures can have different effects on inflammation. Specifically, some inflammatory cytokines (measurable markers of inflammation in the body) appear to decrease at low pressures like 1.3 ATA, while a different set of cytokines responds better at higher pressures, such as 2.0 ATA. Cytokines are small proteins that play a crucial role in cell signaling, particularly within the immune system. They help regulate inflammation, infection response, and overall immune function. While some cytokines promote inflammation to fight off threats, others help reduce inflammation when it's no longer needed. An imbalance in cytokines - especially excessive inflammatory cytokines - can contribute to chronic inflammation, cardiovascular disease, and other health issues. In this study, we are testing an intermediate pressure - 1.75 ATA - to see if we can target both sets of cytokines at once. If successful, this approach could offer broader anti-inflammatory benefits. We are also interested in how this intermediate pressure may improve VO₂ max, a key indicator of cardiovascular fitness. Since VO₂ max is strongly linked to heart health and overall longevity, finding a safe and effective way to improve it has meaningful implications not just for athletes, but for anyone looking to enhance their fitness and well-being.

Recruiting
Has No Placebo

ATX Hyperbarics (+1 Sites)

Image of University of New Brunswick in Fredericton, Canada.

Mediterranean Diet for Toddler Health

24 - 36
All Sexes
Fredericton, Canada

Toddlerhood (ages 2-3) is a critical window when the gut microbiome is still developing and eating habits are being established. Yet, many Canadian toddlers eat diets high in sugar and salt, which may affect long-term health. This study will test whether a MED diet can improve dietary inflammation, gut health, and body composition in toddlers and whether a tailored nutrition education program for parents can help families maintain healthy eating patterns. In this study, toddlers will be randomly assigned to a 3-week MED diet or their usual diet. Families in the MED diet group will receive free meal boxes for the 3 weeks, plus guidance from a nutrition researcher through a structured education program. The standard diet group will continue their regular diet with general nutrition advice. Researchers will collect dietary information, body composition assessments, and stool samples to measure gut microbiome composition and metabolites. This first study of a controlled diet intervention in toddlers, combining behavioral support, high-quality food provision, and advanced gut microbiome analysis, will help understand how early diet shapes lifelong eating habits and health, guiding public health strategies and precision nutrition approaches to prevent chronic disease from early life.

Waitlist Available
Has No Placebo

University of New Brunswick

Dr. Maryam Kebbe, PhD, CLC

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

Recruiting
Has No Placebo

UConn Health

Cutter Lindbergh, Ph.D.

Image of Department of Nutritional Sciences in Storrs, United States.

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

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Image of University of California, San Diego Altman Clinical and Translational Research Institute in San Diego, United States.

Mediterranean Diet for Inflammation Post-Colonoscopy

18+
All Sexes
San Diego, CA

This study aims to investigate the impact of various healthy diets, specifically a modified plant-based Mediterranean diet, on the gut microbiome and overall well-being post-colonoscopy. The investigators hypothesize that certain diets can positively influence gut bacteria, reducing inflammation and enhancing metabolic signals. To explore this, they will utilize metagenomic testing on stool samples to analyze the DNA of gut microorganisms. Additionally, they will conduct immune profiling on serum samples and perform metabolomic analysis to comprehensively evaluate the diet-induced changes in immune response and metabolic pathways. This multi-faceted approach will help them understand how dietary changes affect the composition and function of the gut microbiome, immune function, and overall metabolism.

Waitlist Available
Has No Placebo

University of California, San Diego Altman Clinical and Translational Research Institute

Image of Montana State University in Bozeman, United States.

Haskap Berries for Gut Health

35 - 65
All Sexes
Bozeman, MT

Polyphenol-rich Haskap berries (Haskap) have untapped therapeutic potential to improve human health, and agricultural producers in northern U.S. states are poised to increase production if consumer demand increases. A critical knowledge gap is that little is known about the interactions between gut microbes and Haskap polyphenols to produce bioactive metabolites linked to downstream health impacts. Additionally, little is known about which Haskap varieties and harvest timing yield the greatest bioactive potential. This study aims to address these gaps by investigating the interaction of bioactive components in Haskap with gut microbiota and the resultant gut and serum metabolites, inflammation, and metabolic health, and then couple this with analysis of berries from different Haskap varieties and harvest times.

Recruiting
Paid Trial

Montana State University

Mary P Miles, PhD

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