News / Press Release

What are the Types of INDs?

September 15, 2017
Types of IND Applications

A potential new drug needs IND approval to enter the clinical investigation part of development. IND approval must be completed before the new drug application can be submitted for approval to market to doctors and patients. IND applications must contain three types of information:

With a completed application, the FDA has up to 30 days to review this information and issue an IND. After that, clinical trials can begin.


Types of INDs

An IND is required in the development of a new drug, but there are other types of INDs issued by the FDA:

Emergency Use IND — The FDA may authorize the use of an experimental drug for patients who do not fit the study criteria or as treatment in a life-threatening situation when there is no time to wait for an IND.

Investigator IND — Submitted by a doctor for research on an un-approved drug or a new indication for an approved drug. The FDA approves the doctor who submitted this application to administer the drug and conduct the investigation.

Treatment IND — this allows an experimental drug to be used to treat a patient while the FDA is conducting its review of the drug. It is only approved for serious or life-threatening conditions.

About Translational Drug Development (TD2)

TD2 is an oncology development organization that provides innovative services for oncology-focused companies. Using a dedicated team of professionals with broad experience and understanding in drug development, TD2 is uniquely positioned to support improved and accelerated development of medicines for life-threatening oncology diseases. TD2 applies rigorous and high-throughput translational preclinical development, combined with regulatory affairs expertise, to customize clinical trial design and execution. TD2’s suite of capabilities encourages the timely selection of patient populations who are most likely to benefit from a new agent, and the rapid identification of clinically significant endpoints. TD2 is committed to reducing the risks and uncertainty inherent in the drug development process and to the acceleration of patient access to promising treatments. For more information, visit www.TD2inc.com.

About TD2

TD2 is an oncology development organization that provides innovative services for oncology-focused companies. Using a dedicated team of professionals with broad experience and understanding in drug development, TD2 is uniquely positioned to support improved and accelerated development of medicines for life-threatening oncology diseases. TD2 applies rigorous and high-throughput translational preclinical development, combined with regulatory affairs expertise, to customize clinical trial design and execution. TD2’s suite of capabilities encourages the timely selection of patient populations who are most likely to benefit from a new agent, and the rapid identification of clinically significant endpoints. TD2 is committed to reducing the risks and uncertainty inherent in the drug development process and to the acceleration of patient access to promising treatments. For more information, visit www.TD2inc.com.

Contact
Tara Franks
602-358-8322
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