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Exam Number : PEGACUIS71V1
Exam Name : Pega Certified UI Specialist (CUIS) 71V1
Vendor Name : Pegasystems
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Pegasystems (CUIS) exam Questions

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Sanofi to showcase information from its transformative oncology pipeline at 2021 ASCO assembly

Sanofi to show off statistics from its transformative oncology pipeline at 2021 ASCO meeting Early clinical records for investigational oral selective estrogen receptor (SERD), amcenestrant, demonstrate expertise to become a new endocrine backbone remedy in ER+ HER2- breast cancerData that fortify Libtayo® (cemiplimab-rwlc) as a common of care in superior non-melanoma dermis melanoma and advanced non-small telephone lung melanoma, including new statistics in historically underrepresented patients with brain metastasesLonger time period statistics and new analyses for Sarclisa® (isatuximab-irfc) further beef up efficacy profile, including for elderly sufferers and sufferers with excessive-chance cytogenetic abnormalities PARIS – may additionally 19, 2021 – New analysis being presented at the upcoming virtual American Society of medical Oncology (ASCO) Annual meeting from June four-eight highlights Sanofi’s transformative science and dedication to affected person care across tricky-to-treat cancers, including numerous myeloma, epidermis, lung and breast cancers.“Our pipeline of imaginitive investigational medicines continues to expand, helping our aim to handle essential gaps in medication options for sufferers with cancers of high unmet want,” says Peter C. Adamson, global construction Head, Oncology at Sanofi. “We seem to be ahead to proposing the latest records throughout our oncology portfolio and pipeline in four key areas – multiple myeloma, epidermis cancers, lung cancers and breast cancer, including statistics helping the knowledge for amcenestrant to develop into a most fulfilling-in-category oral endocrine spine therapy.” Early clinical facts for amcenestrant, our investigational oral selective estrogen receptor degrader (SERD), demonstrate competencies to develop into a brand new endocrine backbone therapy in ER+ HER2- breast cancer* abstract 1058: AMEERA 1: phase 1/2 analyze of amcenestrant (SAR439859), an oral selective estrogen receptor (ER) degrader (SERD), with palbociclib (palbo) in postmenopausal ladies with ER+/human epidermal increase factor receptor 2-bad (HER2−) metastatic breast melanoma (MBC) summary TPS1104: AMEERA-5: A randomized, double-blind part three analyze of amcenestrant (SAR439859) + palbociclib versus letrozole + palbociclib for previously untreated ER+/HER2- advanced breast melanoma (Trial in progress) click here to read the whole amcenestrant records press unlock issued by means of Sanofi. statistics analyses fortify Libtayo® (cemiplimab-rwlc) as a typical of care in superior non-melanoma dermis melanoma indications and in superior non-small phone lung melanoma, including new facts in historically underrepresented sufferers with mind metastases Libtayo in Non-melanoma dermis cancer summary 9547: Checkpoint inhibition in immunosuppressed or immunocompromised sufferers with superior cutaneous squamous phone carcinoma (CSCC): information from prospective CemiplimAb-rwlc Survivorship and Epidemiology (C.A.S.E.) studyAbstract 9566: health-connected nice of life (HRQoL) in sufferers (pts) with in the community advanced basal cellphone carcinoma (laBCC) handled with cemiplimab: evaluation of a section II, open-label medical trialAbstract e18830: budget have an impact on (BI) evaluation of cemiplimab-rwlc for advanced basal cellphone carcinoma (BCC) after hedgehog inhibitor (HHI) remedy within the united states different Sanofi stories in Non-Melanoma dermis cancer abstract e18740: Frequency, features, and subsequent treatment (Tx) of actual-world sufferers (pts) who discontinue hedgehog inhibitors (HHI) as first-line (1L) systemic Tx for superior basal mobile carcinoma (aBCC)summary e18742: consequences in sufferers (pts) with advanced basal mobile carcinoma (aBCC) who discontinued hedgehog inhibitors (HHI) as first-line (1L) systemic remedy (Tx) in a US community oncology surroundings: A retrospective observational analyze Libtayo in Non-small cellphone Lung melanoma summary 9085: Cemiplimab monotherapy as first-line (1L) medication of patients with mind metastases from superior non-small cell lung cancer (NSCLC) with programmed telephone death-ligand 1 (PD-L1) ≥50%; EMPOWER-Lung 1 subgroup analysisAbstract 9078: affected person-pronounced signs, functioning, and high-quality of life (QoL) in patients treated with cemiplimab monotherapy for first-line remedy of advanced NSCLC with PD-L1 ≥50%: results from EMPOWER-Lung 1 studyAbstract e18817: budget affect (BI) evaluation of cemiplimab for first-line (1L) superior non-small cellphone lung melanoma (NSCLC) with programmed cellphone death-ligand 1 (PD-L1) ≥50% within the United StatesAbstract e21091: community meta-evaluation (NMA) of immuno-oncology (IO) monotherapy (mono) as first-line (1L) remedies (txs) for superior non-small mobilephone lung cancer (NSCLC) with PD-L1 expression ≥50% Libtayo is being collectively developed via Sanofi and Regeneron below a world collaboration contract. longer term statistics and new analyses for Sarclisa® (isatuximab-irfc) further toughen its efficacy profile, including for aged patients and sufferers with high-risk cytogenetic abnormalities summary 8017: Updates from ICARIA-MM, a section 3 look at of isatuximab (Isa) plus pomalidomide and low-dose dexamethasone (Pd) versus Pd in relapsed and refractory numerous myeloma (RRMM)abstract 8042: Isatuximab plus carfilzomib and dexamethasone in relapsed multiple myeloma sufferers with excessive-possibility cytogenetics: IKEMA subgroup analysisAbstract 8026: Isatuximab plus carfilzomib and dexamethasone versus carfilzomib and dexamethasone in aged sufferers with relapsed multiple myeloma: IKEMA subgroup analysisAbstract e20015: Isatuximab plus carfilzomib and dexamethasone in East Asian sufferers with relapsed diverse myeloma: IKEMA subgroup analysisAbstract 8034: Isatuximab plus carfilzomib and dexamethasone in patients with relapsed assorted myeloma based on prior lines of medication and refractory repute: IKEMA subgroup evaluation Biomarker analysis for tusamitamab ravtansine, an early-stage, abilities first-in-type investigational anti-CEACAM5 antibody drug conjugate for advanced non-small phone lung cancer* summary e21030: Validation of an immunohistochemical assay, CEACAM5 IHC 769, below construction for use with the antibody-drug conjugate tusamitamab ravtansine (SAR408701) protection, pharmacokinetic and pharmacodynamic information with our investigational transforming increase element beta (TGF-b)* abstract 2510: defense, pharmacokinetic and pharmacodynamic consequences from dose escalation of SAR439459, a TGFβ inhibitor, as monotherapy or in mixture with cemiplimab in a section 1/1b look at Early records with investigational anti-ICOS antibody, KY1044, submitted by using Kymab, a Sanofi enterprise* summary 2624: A section 1/2 open-label study of KY1044, an anti-ICOS antibody with dual mechanism of action, as single agent and in combination with atezolizumab, in adult sufferers with superior malignanciesAbstract 2626: KY1044 to goal the ICOS pathways inducing intratumoral Treg depletion and agonism of effector T cells: Preliminary pharmacodynamic markers from a section 1/2 multicenter trial independent research supported via Sanofi Jevtana (Cabazitaxel) abstract 5059First results from a randomized part II study of cabazitaxel (CBZ) versus an androgen receptor targeted agent (ARTA) in patients with bad-prognosis castration-resistant prostate cancer (mCRPC)abstract 1008Randomised multicentre trial of 3 weekly Cabazitaxel versus weekly Paclitaxel chemotherapy in the first line remedy of HER2 negative metastatic breast cancer (MBC)summary e17027Prostate cancer intensive, non-pass reactive therapy (PRINT) for CRPC: meantime analysis of efficacy endpoints click right here to view these abstracts together with the complete digital software observed in the ASCO assembly Library. *These property are presently beneath investigation and their defense and efficacy has not been wholly evaluated by means of any health authority. About Sanofi Sanofi is dedicated to assisting individuals through their fitness challenges. we're a worldwide biopharmaceutical company focused on human health. We stay away from affliction with vaccines, supply imaginative remedies to combat ache and ease struggling. We stand by means of the few who suffer from infrequent illnesses and the thousands and thousands with long-time period chronic conditions. With more than a hundred,000 individuals in a hundred countries, Sanofi is transforming scientific innovation into healthcare options all over. Sanofi, Empowering existence Sanofi Media family members Contact Sally Bain Tel.: +1 (781) 264-1091Sally.Bain@sanofi.com Sanofi Investor members of the family Contacts ParisEva Schaefer-JansenArnaud Delepine Sanofi Investor relations Contacts North AmericaFelix LauscherFara BerkowitzSuzanne Greco Sanofi IR leading line:Tel.: +33 (0)1 fifty three 77 forty five 45investor.members of the family@sanofi.comhttps://www.sanofi.com/en/investors/contact Sanofi forward-looking StatementsThis press unlock contains forward-looking statements as described in the private Securities Litigation Reform Act of 1995, as amended. forward-searching statements are statements that aren't old statistics. These statements include projections and estimates and their underlying assumptions, statements regarding plans, goals, intentions and expectations with admire to future financial effects, activities, operations, features, product construction and competencies, and statements regarding future performance. forward-looking statements are commonly recognized through the phrases “expects”, “anticipates”, “believes”, “intends”, “estimates”, “plans” and an identical expressions. youngsters Sanofi’s management believes that the expectations reflected in such ahead-looking statements are within your budget, buyers are counseled that ahead-looking counsel and statements are field to a considerable number of dangers and uncertainties, many of that are difficult to foretell and generally beyond the handle of Sanofi, that could trigger exact effects and developments to vary materially from these expressed in, or implied or projected with the aid of, the ahead-looking counsel and statements. These risks and uncertainties encompass amongst other issues, the uncertainties inherent in analysis and construction, future medical information and analysis, together with put up marketing, choices with the aid of regulatory authorities, such as the FDA or the EMA, regarding whether and when to approve any drug, device or organic utility that may well be filed for such a product candidates in addition to their selections involving labelling and different concerns that may affect the availability or industrial skills of such product candidates, the undeniable fact that product candidates if authorised might also now not be commercially a success, the future approval and industrial success of therapeutic alternate options, Sanofi’s means to benefit from exterior growth alternatives, to complete connected transactions and/or reap regulatory clearances, dangers linked to intellectual property and any connected pending or future litigation and the gold standard outcome of such litigation, developments in change costs and prevailing hobby quotes, volatile economic and market conditions, can charge containment initiatives and subsequent alterations thereto, and the have an effect on that COVID-19 could have on us, our valued clientele, suppliers, companies, and other company companions, and the economic situation of any one of them, as well as on our employees and on the global financial system as an entire. Any fabric effect of COVID-19 on any of the foregoing may also adversely impact us. This condition is changing hastily and additional influences may additionally come up of which we aren't currently conscious and might exacerbate other prior to now recognized hazards. The risks and uncertainties also encompass the uncertainties mentioned or recognized within the public filings with the SEC and the AMF made by way of Sanofi, together with these listed under “risk elements” and “Cautionary statement related to ahead-looking Statements” in Sanofi’s annual record on form 20-F for the year ended December 31, 2020. other than as required through applicable legislation, Sanofi doesn't undertake any obligation to update or revise any ahead-searching suggestions or statements. Attachment Press liberate




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