We've found
9,144
archived clinical trials in
Ocular
We've found
9,144
archived clinical trials in
Ocular
Evaluating NeuroVision's Neural Vision Correction (NVC) Myopia Treatment
Updated: 12/31/1969
Evaluating the Efficacy of NeuroVisions's NVC Treatment for Low Myopia
Status: Enrolling
Updated: 12/31/1969
Evaluating NeuroVision's Neural Vision Correction (NVC) Myopia Treatment
Updated: 12/31/1969
Evaluating the Efficacy of NeuroVisions's NVC Treatment for Low Myopia
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Updated: 12/31/1969
A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program
Status: Enrolling
Updated: 12/31/1969
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Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Updated: 12/31/1969
Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Status: Enrolling
Updated: 12/31/1969
Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Updated: 12/31/1969
Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Status: Enrolling
Updated: 12/31/1969
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Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Updated: 12/31/1969
Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Status: Enrolling
Updated: 12/31/1969
Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Updated: 12/31/1969
Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Status: Enrolling
Updated: 12/31/1969
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Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Updated: 12/31/1969
Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Status: Enrolling
Updated: 12/31/1969
Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Updated: 12/31/1969
Texan Allergy & Sinus Center Mountain Cedar Intra-Lymphatic Immunotherapy Study
Status: Enrolling
Updated: 12/31/1969
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Efficacy Study of Ketorolac and HPMC to Treat Dry Eye
Updated: 12/31/1969
A Double-Masked, Randomized, Single-Center Study Evaluating the Effect of 0.30% Ketorolac/0.80% HPMC, 0.80% HPMC and Vehicle on Symptoms of Dry Eye After Exposure to the Controlled Adverse Environment (CAE)
Status: Enrolling
Updated: 12/31/1969
Efficacy Study of Ketorolac and HPMC to Treat Dry Eye
Updated: 12/31/1969
A Double-Masked, Randomized, Single-Center Study Evaluating the Effect of 0.30% Ketorolac/0.80% HPMC, 0.80% HPMC and Vehicle on Symptoms of Dry Eye After Exposure to the Controlled Adverse Environment (CAE)
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Updated: 12/31/1969
Clinical Evaluation of Etafilcon A Contact Lenses Using a Novel Molding Process 2
Status: Enrolling
Updated: 12/31/1969
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Evaluation of the Efficacy of Topical Ophthalmic Steroids in a Modified Conjunctival Allergen Challenge (CAC) Model
Updated: 12/31/1969
A Phase 4, Randomized, Double-Masked, Single Center, Placebo-Controlled Adaptive Clinical Trial, Using Prednisolone Sodium Phosphate Ophthalmic Solution, 1%, in Subjects With Allergic Conjunctivitis to Evaluate a Modified Conjunctival Allergen Challenge (CAC) Model
Status: Enrolling
Updated: 12/31/1969
Evaluation of the Efficacy of Topical Ophthalmic Steroids in a Modified Conjunctival Allergen Challenge (CAC) Model
Updated: 12/31/1969
A Phase 4, Randomized, Double-Masked, Single Center, Placebo-Controlled Adaptive Clinical Trial, Using Prednisolone Sodium Phosphate Ophthalmic Solution, 1%, in Subjects With Allergic Conjunctivitis to Evaluate a Modified Conjunctival Allergen Challenge (CAC) Model
Status: Enrolling
Updated: 12/31/1969
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Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Versus Alcon Phacoemulsification Machines
Updated: 12/31/1969
Intra-surgical Evaluation of CATS Tonometer Prism and AMO Versus Alcon Phacoemulsification Machines
Status: Enrolling
Updated: 12/31/1969
Intra-surgical Evaluation of CATS Tonometer Prism and Abbott Medical Optics Versus Alcon Phacoemulsification Machines
Updated: 12/31/1969
Intra-surgical Evaluation of CATS Tonometer Prism and AMO Versus Alcon Phacoemulsification Machines
Status: Enrolling
Updated: 12/31/1969
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Evaluation of Visual Performance With Contact Lenses
Updated: 12/31/1969
Evaluation of Visual Performance With Contact Lenses
Status: Enrolling
Updated: 12/31/1969
Evaluation of Visual Performance With Contact Lenses
Updated: 12/31/1969
Evaluation of Visual Performance With Contact Lenses
Status: Enrolling
Updated: 12/31/1969
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Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
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Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
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Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
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Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
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Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
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Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
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Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
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Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
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Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
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Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Updated: 12/31/1969
Design Validation of Senofilcon A With New UV-blocking Additive
Status: Enrolling
Updated: 12/31/1969
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A Study to Evaluate the Safety and Effectiveness of Restylane-Defyne for Punctual Occlusion
Updated: 12/31/1969
A Single-Arm, Single-Center, Randomized, Single-Masked Study to Evaluate Restylane Defyne for Canalicular Occlusion in Participants With Mild to Moderate Dry Eye Disease
Status: Enrolling
Updated: 12/31/1969
A Study to Evaluate the Safety and Effectiveness of Restylane-Defyne for Punctual Occlusion
Updated: 12/31/1969
A Single-Arm, Single-Center, Randomized, Single-Masked Study to Evaluate Restylane Defyne for Canalicular Occlusion in Participants With Mild to Moderate Dry Eye Disease
Status: Enrolling
Updated: 12/31/1969
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A Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Updated: 12/31/1969
A Long Term Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Status: Enrolling
Updated: 12/31/1969
A Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Updated: 12/31/1969
A Long Term Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Status: Enrolling
Updated: 12/31/1969
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A Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Updated: 12/31/1969
A Long Term Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Status: Enrolling
Updated: 12/31/1969
A Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Updated: 12/31/1969
A Long Term Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Status: Enrolling
Updated: 12/31/1969
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A Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Updated: 12/31/1969
A Long Term Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Status: Enrolling
Updated: 12/31/1969
A Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Updated: 12/31/1969
A Long Term Follow-up Study to Evaluate the Safety of RetinoStat® in Patients With Age-Related Macular Degeneration
Status: Enrolling
Updated: 12/31/1969
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Clinical Evaluation of Fitting Investigational Contact Lenses Phase 2
Updated: 12/31/1969
Clinical Evaluation of Fitting Investigational Contact Lenses Phase 2
Status: Enrolling
Updated: 12/31/1969
Clinical Evaluation of Fitting Investigational Contact Lenses Phase 2
Updated: 12/31/1969
Clinical Evaluation of Fitting Investigational Contact Lenses Phase 2
Status: Enrolling
Updated: 12/31/1969
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Efficacy and Safety Study of IBI-10090 in Patients Undergoing Cataract Surgery
Updated: 12/31/1969
A Multicenter, Randomized, Double-masked, Dose-ranging, Phase 2 Study to Evaluate the Efficacy and Safety of IBI-10090 in Cataract Surgery Patients
Status: Enrolling
Updated: 12/31/1969
Efficacy and Safety Study of IBI-10090 in Patients Undergoing Cataract Surgery
Updated: 12/31/1969
A Multicenter, Randomized, Double-masked, Dose-ranging, Phase 2 Study to Evaluate the Efficacy and Safety of IBI-10090 in Cataract Surgery Patients
Status: Enrolling
Updated: 12/31/1969
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