Examples of Amgen IP in a sentence
During the Preclinical R&D Term for each Collaboration Program, Amgen hereby grants to EnteraBio a non-exclusive, worldwide, royalty-free right under Amgen IP solely to conduct Preclinical Research & Development as contemplated to be performed by EnteraBio under each Work Plan.
However, Amgen reserves the unilateral right, at its sole discretion, to determine whether to supply Amgen (IP), and by what mechanism, after termination of the trial and before it is available commercially.
On a Program-by-Program basis, during the applicable Preclinical Development Term, Amgen hereby grants to Kite a non-exclusive, worldwide, royalty-free right under Amgen IP solely to conduct Preclinical Development as contemplated under the applicable Preclinical Development Plan.
However, Amgen reserves the unilateral right, at its sole discretion, to determine whether to supply Amgen IP and by what mechanism, after termination of the study and before the product(s) is/are available commercially.
The toxicity grading scale used in this study is described in Appendix A.The investigator must assess whether the adverse event is possibly related to Amgen IP: evolocumab and/or other protocol-required therapies.
This relationship is indicated by a “yes” or “no” response to the question: Is there a reasonable possibility that the event may have been caused by Amgen IP: evolocumab and/or other protocol-required therapies?The investigator must assess whether the adverse event is possibly related to the Amgen device: Prefilled AI/Pen or 3.5 mL AMD/ Personal Injector used to administer (evolocumab) IP.
Large competitors such as Valeo and Nissens have strong brands and in order to compete it is important to NRF to own a strong well-known brand.
Amgen will have the sole right but not the obligation, at its own cost, for preparing, filing, prosecuting (including provisional, reissue, continuing, continuation-in-part, and substitute applications and any foreign counterparts thereof), and maintaining all Patents within the Amgen IP and the Collaboration IP (collectively, the “Amgen Prosecuted Patents”) and conducting any interferences and oppositions or similar proceedings relating to the Amgen Prosecuted Patents.
Serious adverse events reported outside of the protocol-required reporting period will be captured within the safety database as clinical trial cases for the purposes of expedited reporting.The investigator must assess whether the serious adverse event is possibly related to Amgen IP: evolocumab or other protocol-required therapies.
The investigator is to notify the IRB/IEC in writing of the study’s completion or early termination (ET) and send a copy of the notification to Amgen.Subjects may be eligible for continued treatment with Amgen IP by an extension protocol or as provided for by the local country’s regulatory mechanism.