CRISPR Therapeutics to Participate in the Guggenheim Healthcare Talks 2021 Oncology Day

On February 5, 2021 CRISPR Therapeutics (Nasdaq: CRSP), a biopharmaceutical company focused on creating transformative gene-based medicines for serious diseases, reported that members of its senior management team are scheduled to participate in the Guggenheim Healthcare Talks 2021 Oncology Day on Friday, February 12, 2021, at 3:30 p.m. ET (Press release, CRISPR Therapeutics, FEB 5, 2021, View Source [SID1234574675]).

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A live webcast of the event will be available on the "Events & Presentations" page in the Investors section of the Company’s website at View Source A replay of the webcast will be archived on the Company’s website for 14 days following the presentation.

Bristol Myers Squibb to Participate in Guggenheim’s Virtual Healthcare Talks

On February 5, 2021 Bristol Myers Squibb (NYSE: BMY) reported that the company will take part in a fireside chat at Guggenheim’s Virtual Healthcare Talks | 2021 Oncology Day, which will be webcast on Friday, February 12, 2021 (Press release, Bristol-Myers Squibb, FEB 5, 2021, View Source;2021-Oncology-Day/default.aspx [SID1234574672]). Chris Boerner, Ph.D., Executive Vice President, Chief Commercial Officer will answer questions about the company at 12 p.m. ET.

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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Investors and the general public are invited to listen to a live webcast of the session at View Source Material related to the company’s presentation will be available at the same website at the start of the live webcast. An archived edition of the session will be available later that day.

Ipsen to showcase commitment to going beyond traditional outcome measures for patients living with renal cell carcinoma at ASCO GU 2021

On February 5, 2021 Ipsen (Euronext: IPN; ADR: IPSEY) reported that new data from its growing oncology portfolio will be presented at the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Genitourinary Cancers Symposium (ASCO GU), taking place virtually from 11-13 February 2021 (Press release, Ipsen, FEB 5, 2021, View Source [SID1234574671]).11 A total of 10 abstracts spanning several genitourinary cancers including advanced RCC, and metastatic, castration-resistant prostate cancer (mCRPC), highlight the utility of Ipsen’s medicines and its commitment to advancing patient care.1-10

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"The presentations showcased at ASCO (Free ASCO Whitepaper) GU exemplify Ipsen’s commitment to prioritize outcome measures which directly impact patients’ lives," said Amauri Soares, Vice President, Medical Affairs Oncology, Ipsen. "New data from the Phase III CheckMate -9ER trial highlight how first-line treatment with the combination of cabozantinib and nivolumab has the potential to extend the lives of patients living with advanced RCC without having to compromise on quality of life compared with sunitinib. We’re looking forward to sharing these data with the medical community at ASCO (Free ASCO Whitepaper) GU and bringing this important treatment option to patients at the earliest opportunity."

Highlights from key data on Ipsen medicines to be presented during the ASCO (Free ASCO Whitepaper) GU 2021 Symposium include:

Extended follow-up outcomes data from the CheckMate -9ER study including patients living with advanced RCC and sarcomatoid features (sRCC) – an aggressive histologic subtype associated with poor prognoses1
Patient reported outcomes of patients living with advanced RCC – additional analysis from the CheckMate -9ER study of the combination of Cabometyx (cabozantinib) with Opdivo (nivolumab) versus sunitinib2
A comparative, retrospective real-world evidence study suggesting Cabometyx (cabozantinib) was associated with a significantly higher response rate versus other TKIs (axitinib, lenvatinib, pazopanib, sorafenib, sunitinib) in patients living with metastatic renal cell carcinoma (mRCC) following checkpoint inhibitor (CPI) treatment3
Findings from a study using machine learning to explore the potential synergistic effects of Cabometyx (cabozantinib) and a programmed cell death protein 1 (PD1) inhibitor in mRCC4
Trial design of the Phase III randomized, open-label CONTACT-02 study of Cabometyx (cabozantinib) plus Tecentriq (atezolizumab) versus second novel hormone therapy (NHT) in patients living with mCRPC5

Precision BioSciences to Present at Guggenheim Healthcare Talks 2021 Oncology Day

On February 4, 2021 Precision BioSciences, Inc. (Nasdaq: DTIL) a clinical stage biotechnology company dedicated to improving life with its proprietary ARCUS genome editing platform, reported it will participate in the Guggenheim Healthcare Talks 2021 Oncology Day on February 11, 2021 at 2:00 PM ET (Press release, Precision Biosciences, FEB 4, 2021, View Source [SID1234576689]).

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A live webcast of the presentation will be accessible on the Company’s website, www.precisionbiosciences.com, in the Investors & Media section under Events and Presentations. An archived replay of the webcasts will be available for approximately 30 days following the presentation.

Cornell startup raises $44M to advance ‘C Dots’ biotech

On February 4, 2021 Elucida Oncology, a biotechnology company based on C Dots – ultra-small nanoparticles developed at Cornell that show promise in identifying and fighting cancer – reported that secured $44 million in financing, in addition to $28 million raised in 2018 (Press release, Elucida Oncology, FEB 4, 2021, View Source [SID1234575245]).

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A rendering of the molecular structure of a Cornell dot, which is smaller than 10 nanometers.
C Dots, originally called Cornell dots, were created more than 15 years ago in the lab of Uli Wiesner, the Spencer T. Olin Professor of Engineering in the Department of Materials Science and Engineering. Wiesner has been working to put C Dots to use in the fight against cancer ever since.

As a result of their size, C Dots proved safe and effective for use in human beings as both an imaging and a diagnostic tool in early clinical studies. The new funding will help the company gain regulatory approval as a targeted cancer therapeutic, and to expand its management team and its laboratory capabilities.

"This vote of support from investors means a lot to me," Wiesner said. "Given C Dots’ broad applicability, I have been pushing efforts in health care-focused startups since 2005 to commercialize this technology. At the beginning it was a reagent company. Then we started a company focusing on diagnostics, and now we have a company emphasizing therapeutics."

This evolution shows the flexibility and the value of the C Dot platform, he said.

Elucida was founded in 2014 and co-founders include Wiesner, Kai Ma, Ph.D. ’15, and Dr. Michelle Bradbury, director of intraoperative imaging at Memorial Sloan Kettering Cancer Center and professor of radiology at Weill Cornell Medicine.

In the C Dots, each silica-based nanoparticle has an embedded fluorescent molecule in the interior for optical detection, as well as several organic ligands and functional groups on the surface. This makes the C Dot platform more flexible: Specific ligands prevent attack from the body’s defenses, while targeting groups cause the C Dot to specifically bind with tumor cells when they come into contact.

In this configuration, C Dots are currently being tested as a diagnostic tool in ongoing clinical trials at Memorial Sloan Kettering and Weill Cornell Medicine. When they are injected into a person with cancer, the glowing C Dots attach to cancer cells and can be seen by the surgeon with the use of a fluorescent camera.

In order to gain regulatory approval as a targeted cancer therapeutic, the company will need to complete ongoing toxicology studies and file an Investigational New Drug application with the Food and Drug Administration, according to Geno Germano, CEO and president of Elucida. The latest round of funding will support these moves.

"We have an excellent technology, an incredible team at Elucida, and a world-class board to help us navigate the highly complex landscape around cancer therapeutics," Wiesner said.

Elucida is planning to start clinical trials this summer; by the spring of 2022, the company expects to have the first data from those trials.

"If this trial validates our therapeutic approach the way we think and hope it will," Wiesner said, "our C Dot nanoparticle platform will give us a whole battery of disease-fighting products."

Chris Dawson is a writer for the College of Engineering.