Clinical Trials

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Clinical trials are conducted to collect data regarding the safety and efficacy of new drug and device development. Treatments studied in clinical trials might be new drugs or new combinations of drugs, new surgical procedures or devices, or new ways to use existing treatments. Office visits, lab test, medication, study related procedures, and compensation for time and travel are provided to eligible participants.


CURRENT CLINICAL STUDIES

Chronic Rhinosinusitis:

A Phase II, Patient blinded, Two-part, Randomized, Parallel-group Trial to Evaluate the Safety, Tolerability, Pharmacokinetic, and Efficacy of LYR-220 in Chronic Rhinosinusitis (CRS) Patients Who Have Had a Prior Ethmoidectomy

To see if you qualify or for more information call 210-545-0404 ext. 1324 and reference clinical study LYR-220-2021-001

Phase III, Randomized, Blinded, Controlled, Parallel-Group Trial to Evaluate the Efficacy and Safety of LYR-210 for the Treatment of Chronic Rhinosinusitis (CRS) in Adults

To see if you qualify or for more information call 210-545-0404 ext. 1324 and reference clinical study LYR-210-2021-004


TINNITUS:

The purpose of this study is to test the effectiveness, safety, and tolerability of the investigational product, OTO-313, compared to placebo in people with unilateral tinnitus (the perception of ringing or noise in one ear).

To see if you qualify or for more information call 210-545-0404 ext. 1324 and reference clinical study OTO-313-201:


HEARING LOSS:

This is a Phase 2, prospective, randomized, double-bling, placebo-controlled, single-dose, multicenter study to evaluate the efficacy of FX-322, administered by intratympanic injection, in adults with acquired sensorineural hearing loss (SNHL). Previous human studies in subjects 18 to 65 years inclusive (FX-322-103, FX-322-201, FX-322-111) and subjects inclusive (FX-322-112) demonstrated that a single dose FX-322 was well tolerated in patients with acquired SNHL with no treatment-related serious adverse events.

To see if you qualify or for more information call 210-545-0404 ext. 1324 and reference clinical study FX-322-208:

 


CHRONIC TYMPANIC MEMBRANE PERFORATION

A Phase 1/2, Randomized, Placebo-controlled Study to Asses the Safety, Tolerability, Efficacy, and Pharmacokinetics of ASP0598 Otic Solution Following Topical Application into the Ear in Subjects with Chronic Tympanic Membrane Perforation (CTMP)

To see if you qualify or for more information call 210-545-0404 ext. 1324 and reference clinical study ASTELLAS-0598-CL-0101

Our team can answer questions, discuss your needs and help locate research studies that match your interests. We can also provide interpreter services for non-English speaking patients.

 


CLINICAL RESEARCH TEAM

Primary Investigator: Dr. Jeffrey Rosenbloom
Sub Investigator: Dr. Benjamin Webb
Senior Research Coordinator: Robert Gonzalez, LVN
Phone: 210-545-0404 ext. 1324
Clinical Research Coordinator: Frank Morales, MA
Phone: 210-545-0404 ext. 1328

Alamo ENT Clinical Trials
Alamo ENT Clinical Trials