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Albiruni Ryan Abdul Razak

Researcher at Princess Margaret Cancer Centre

Publications -  253
Citations -  7154

Albiruni Ryan Abdul Razak is an academic researcher from Princess Margaret Cancer Centre. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 39, co-authored 195 publications receiving 5045 citations. Previous affiliations of Albiruni Ryan Abdul Razak include Harvard University & University Health Network.

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Abstract CT116: First-in-human study of AZD8853, an anti-growth and differentiation factor 15 (GDF15) antibody, in patients (pts) with advanced/metastatic solid tumors

TL;DR: CARNEIRO et al. as mentioned in this paper presented a Phase I/IIa, first-in-human, open-label study (NCT05397171) assessing the safety, pharmacokinetics (PK), pharmacodynamics (PD) and preliminary efficacy of AZD8853 in pts with histologically or cytologically confirmed locally advanced, unresectable or metastatic mismatch repair-proficient colorectal cancer (pMMR-CRC), non-small-cell lung cancer (NSCLC) and urothelial carcinoma (UC).
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Phase 1b study of weekly split-dose selinexor in soft tissue sarcoma (STS).

TL;DR: Split-dose selinexor was well tolerated in this heterogeneous group of pts with advanced STS and warrants further interrogation, and Updated toxicity, safety, efficacy and QoL data will be presented at the meeting.
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Phase 1 study of GSK3368715, a type I PRMT inhibitor, in patients with advanced solid tumors

TL;DR: GSK3368715, a first-in-class reversible inhibitor of type I protein methyltransferases (PRMTs), demonstrated anticancer activity in preclinical studies as mentioned in this paper .
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Overall survival and long-term safety in patients with advanced gastrointestinal stromal tumor previously treated with imatinib: Updated analyses from INTRIGUE.

TL;DR: The second interim analysis (IA) for overall survival (OS) in the INTRIGUE trial, data were immature (OS event rate, 22.3%), and median OS was not reached in either arm for the KIT exon 11 intent-to-treat (ITT) and all-patient (AP) ITT populations as mentioned in this paper .