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Open Trials

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Cushings Syndrome

Novartis Pharmaceuticals

Ages Eligible for Study: 18 Years to 85 Years (Adult, Senior); Genders Eligible for Study: All; Accepts Healthy Volunteers: No

Recruiting

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FLEX Registry

Agendia

MammaPrint, BluePrint, and Full-genome Data Linked With Clinical Data to Evaluate New Gene EXpression Profiles (FLEX)

Recruiting

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Evaluation of the Effects of Product on the Skin After X Hours/Days*

Estée Lauder

Skin Care Other: Retinol Complex 0.5 Other: Facial cleanser Other: Moisturizing lotion Other: Sunscreen Device: Skin Imaging

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UPCOMING TRIALS

Wondering if a clinical study is appropriate for you? It is with the help of people like you that new and improved medicines are being discovered. By participating, you help in the discovery of a medicine, cures and treatments for the future and eventually the betterment of the society.

Listed below are some upcoming research areas where you could potentially join:

INTERESTED?

FREQUENTLY ASKED QUESTIONS

Clinical trials are the first step in bringing new treatment options to people around the world. Individuals like you, who participate in clinical trials, make it possible to advance medicine. Effective and safe new treatments and cures can only become realities if people take the initiative to participate in a clinical research study. When a trial is complete, researchers better understand how a medication benefits a specific medical condition.
By participating in a research study, not only are you helping researchers understand how a new medication works, but you are bringing new treatment options to people around the world to improve their health and well-being. You also have the potential to receive innovative treatment under the supervision of your trusted physician at no cost.
Before participating in a study, participants are provided information about the study and are given the chance to ask questions. This process is called Informed Consent. The purpose of the informed consent process is to make sure participants are adequately informed of important details about the clinical study so they can make an informed choice about their participation. Informed consent begins before a research volunteer agrees to participate in a trial and continues throughout the study.

Join your hand in making clinical research better.

You are doing a great job in helping accelerate clinical research for patients in need of live saving treatments.

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