There hasn't been any new medication for OCD since 1997. Obsessive Compulsive is studying an investigational medication that modulates glutamate, and we want you to know more.
If you suffer from obsessive-compulsive disorder (OCD), a clinical trial may be able to help. We are studying an investigational drug to help treat the symptoms of OCD. If you are between the ages of 18 and 65 years old and suffer from the symptoms of OCD, you may qualify. There is no cost to you to participate and insurance is not required.
Learn more about the benefits of joining our OCD clinical trial and see if you qualify today!
Before a medication can be approved for treatment, it needs to be tested in a clinical study to evaluate the safety and efficacy of the drug.
Clinical trials take place in medical centers around the world, and involve volunteers helping doctors to look at new ways to treat conditions.
Clinical trials represent the latest research about your condition, and can offer new treatment options.
If you think you might like to participate in the Chronic Cough Study or would like more information, please enter your information below so we can see if you may qualify and can contact you about the study. Keep in mind that participation is entirely voluntary. If you do decide to take part in the study, you may change your mind about participating at any time.
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Frequetly Asked Question
A Clinical Research Study (also called a clinical trial) is a medical study that helps answer important questions about an investigational drug or device, such as: does it work, or how effective is it compared to another drug/device?All medications must be tested in clinical research studies before they can be approved by regulatory authorities for doctors to prescribe to patients. Without people taking part in these studies, we would have no new treatments. The volunteers who participate in clinical research studies play a major role in helping to advance medicine.
The study team respects and protects the participant’s privacy. The study team will not share the participant’s information except as required by law. The study team will store the participant’s personal information with codes that do not identify the participant. The Informed Consent Form has more information about the participant’s privacy.
Yes, your involvement in the study is voluntary. The participant may stop participating at any time. If the participant decides to stop early, please notify the study team. The study team will ask the participant to return to the study office at least once for follow up tests to check the participant's health once the investigational medication has been stopped.