On January 11, 2022 Quest Diagnostics Incorporated (NYSE: DGX), the world’s leading provider of diagnostic information services, reported that it will report fourth quarter and full year 2021 financial results on Thursday, February 3, 2022, before the market opens (Press release, Quest Diagnostics, JAN 11, 2022, View Source,-2022 [SID1234598581]). It will hold its quarterly conference call to discuss the results beginning at 8:30 a.m. Eastern Time on that day.

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The conference call can be accessed by dialing 888-455-0391 within the U.S. and Canada, or 773-756-0467 internationally, using the passcode: "7895081." The earnings release and live webcast will be posted on www.QuestDiagnostics.com/investor. The company suggests participants dial in approximately 10 minutes before the call.

A replay of the call may be accessed online at www.QuestDiagnostics.com/investor or by phone at 800-839-9317 for domestic callers or 203-369-3605 for international callers; no passcode is required. Telephone replays will be available from approximately 10:30 a.m. Eastern Time on February 3, 2022 until midnight Eastern Time on February 17, 2022.

Anyone listening to the call is encouraged to read the company’s periodic reports on file with the Securities and Exchange Commission, including the discussion of risk factors and historical results of operations and financial condition in those reports.

On January 11, 2022 iTeos Therapeutics, Inc. (the "Company") Presented the Corporate Presentation (Presentation, iTeos Therapeutics, JAN 11, 2022, View Source [SID1234598580]).

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On January 11, 2022 IMMUNOPRECISE ANTIBODIES LTD. ("IPA" or the "Company") (NASDAQ: IPA) (TSXV: IPA), a leader in full-service, therapeutic antibody discovery, reported that on January 7, 2022 its board of directors approved the grant of 170,000 stock options (the "Options") under its stock option plan to acquire up to an aggregate of 170,000 common shares in the capital of IPA ("Common Shares") (Press release, ImmunoPrecise Antibodies, JAN 11, 2022, View Source [SID1234598579]). The Options were granted to certain officers of IPA. Each Option is exercisable for a period of five years from the date of grant at an exercise price of Cdn $7.94 per Common Share. One third of the Options granted to each officer will vest every six months from the date of grant.

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On January 11, 2022 Nascent Biotech, Inc. (OTCQB:NBIO) ("Nascent Biotech", "Nascent", or the "Company"), a clinical-stage biotechnology Company pioneering the development of monoclonal antibodies targeting treatment of various cancers and viral infections, reported the completion of dosing of the second cohort of patients involved in the Company’s Phase I trial to evaluate Pritumumab ("PTB") as a treatment for Brain Cancer, including Malignant Primary Brain Tumors and adult Brain Metastases (Press release, Nascent Biotech, JAN 11, 2022, View Source [SID1234598578]).

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"After reviewing data gathered from the first and second cohorts, this milestone will allow us to quickly advance to our third cohort in the study, which is anticipated to start this month," noted Nascent CEO, Sean Carrick.

PTB is a natural human antibody that works by binding to Cell surface Vimentin (also referred to as ectodomain vimentin, or EDV), a protein expressed on the surface of epithelial cancers. PTB is used as a targeted immunotherapy that, unlike chemotherapy, only targets cancer cells without damaging healthy cells.

Carrick continued, "Having successfully completed the first two cohorts associated with this important trial, we are excited to move to our third escalation. Our rapid progress to this stage, and the positive data trends we have seen in the course of that process, moves us closer to petitioning for approval to begin Phase 2 testing."

Those interested in participating in the trial or finding out more information are invited to visit www.clinicaltrials.gov under the search term "Pritumumab".

On January 11, 2022 Pulse Biosciences, Inc. (Nasdaq: PLSE), a novel bioelectric medicine company commercializing the CellFX System powered by Nano-Pulse Stimulation (NPS) technology, reported preliminary unaudited fourth quarter 2021 financial and operational results (Press release, Pulse Biosciences, JAN 11, 2022, View Source [SID1234598577]).

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Recent Highlights:

Preliminary unaudited full year 2021 revenue is expected to be in the range of $1.3 million to $1.4 million, including preliminary unaudited fourth quarter 2021 revenue of approximately $750 thousand

Completed the first two commercial sales of CellFX Systems in the fourth quarter of 2021

Transitioned 17 Controlled Launch Program participants to commercial use of their acquired CellFX System, bringing the total number of commercial conversions to 29 at the end of the fourth quarter of 2021

Completed onboarding CellFX Controlled Launch Program participants, increasing the total number of program participants to 70. Six clinics have opted out of the program to date.

"We are proud of our accomplishments in 2021," said Darrin Uecker, President and CEO of Pulse Biosciences. "We achieved regulatory approval for the CellFX System in the U.S., Europe and Canada, onboarded Controlled Launch Program participants, expanded commercialization across each geography and continued to advance our clinical and regulatory initiatives. These achievements position Pulse Biosciences to drive meaningful growth in 2022 and beyond as we leverage the full potential of NPS technology in dermatology and other medical specialties."

The Company’s fourth quarter 2021 financial results are preliminary and are subject to the completion of the Company’s 2021 audit. Complete fourth quarter and full year 2021 financial results will be announced in March.