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To prevent this, adopt a rotation system
In the absence of completed and published phase I/II/III clinical trials, it is impossible to establish a complete profile of potential adverse effects in humans
These changes mean clinicians and patients will need to weigh route-specific adherence, side-effect profiles, and total cost of therapy when selecting treatment
These figures validate payer concerns
If a manufacturer or licensing partner is unable to supply us with drugs in a timely manner, we may encounter substantial delays in commencement, enrollment, or completion of our clinical trials or an inability to successfully commercialize any product candidates we may develop
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