Aravive to Present Updated Modeling Data from Batiraxcept Clinical Trials at the AACR Annual Meeting

On March 2, 2022 Aravive, Inc. (Nasdaq: ARAV), a late clinical-stage oncology company developing targeted therapeutics to treat metastatic disease, will present updated exposure-response analyses from the Phase 1b platinum-resistant ovarian cancer and Phase 1b clear cell renal cancer trials at the American Association for Cancer Research (AACR) (Free AACR Whitepaper) annual meeting taking place between April 8-13, 2022 in New Orleans, Louisiana (Press release, Aravive, MAR 2, 2022, View Source [SID1234609352]). The abstract presentation at AACR (Free AACR Whitepaper) will be presented virtually.

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Presentation Details
Title: Exposure-Response Analysis of Batiraxcept and Application to Recommended Phase 2 Dose in Platinum-Resistant Ovarian and Clear Cell Renal Cancers
Abstract Number: 7867
Presentation Type: Remote Poster Presentation
Date: April 8, 2022

Shattuck Labs Announces Participation in Upcoming March Conferences

On March 2, 2022 Shattuck Labs, Inc. (Shattuck) (NASDAQ: STTK), a clinical-stage biotechnology company pioneering the development of bi-functional fusion proteins as a new class of biologic medicine for the treatment of patients with cancer and autoimmune disease, reported that company management will participate in two virtual investor conferences in March 2022 (Press release, Shattuck Labs, MAR 2, 2022, View Source [SID1234609351]).

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Presentation Details

Conference: 42nd Annual Cowen Healthcare Conference
Format: Ovarian Cancer Panel Discussion
Presenter: Lini Pandite, MBChB, M.B.A., Shattuck’s Chief Medical Officer
Date: March 9, 2022
Time: 12:50 p.m. ET

Conference: Oppenheimer’s 32nd Annual Healthcare Conference
Format: Corporate Presentation
Presenter: Conor Richardson, Shattuck’s Senior Director of Finance and Investor Relations
Date: March 15, 2022
Time: 3:20 p.m. ET

A live webcast of both presentations will be available on the Events & Presentations section of the Company’s website. A replay of the webcasts will be archived for up to 90 days following the presentation date.

Surface Oncology Reports Financial Results and Corporate Highlights for Fourth Quarter and Full Year 2021

On March 2, 2022 Surface Oncology (Nasdaq: SURF), a clinical-stage immuno-oncology company developing next-generation immunotherapies that target the tumor microenvironment, reported financial results and corporate highlights for the fourth quarter and full year 2021, as well as anticipated 2022 corporate milestones (Press release, Surface Oncology, MAR 2, 2022, View Source [SID1234609348]).

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"Surface continues to make great progress advancing our portfolio of next-generation antibody therapies, and we are excited to have planned clinical data readouts this year for both our anti-IL-27 antibody, SRF388, and our anti-CD39 antibody, SRF617," said Rob Ross, M.D., chief executive officer. "The need for new medicines to help patients confronting cancer is profound, and it spurs all of us at Surface to advance our programs with urgency and passion. We are encouraged by the momentum of our programs and their potential to become important therapeutic options for a broad spectrum of cancers."

Ross continued, "Today we announced that Geoffrey McDonough, M.D., is stepping down from the Surface board of directors effective immediately. Geoff joined our board in February of 2018, and we thank him for the significant contributions he made during his tenure. While we will miss his leadership and counsel, the board remains vibrant and was further strengthened with the addition of Ben Hickey and the appointment of Denice Torres as board chair late last year."

Fourth Quarter and Subsequent Corporate Highlights:

In December 2021, Surface announced that the U.S. Food and Drug Administration (FDA) had cleared the Investigational New Drug (IND) application for GSK4381562 (formerly SRF813) to proceed into a first-in-human clinical trial. GSK4381562 is a fully human IgG1 antibody targeting PVRIG (also known as CD112R), an inhibitory protein expressed on natural killer cells (NK cells) and T cells. Surface will receive a $30 million milestone payment in conjunction with the initiation of the first Phase 1 study for GSK4381562 and is eligible to receive an additional $700 million in future milestone payments, as well as be eligible to receive tiered royalties on global net sales.

In December 2021, Surface presented results from a first-in-human dose-escalation study of SRF617 at the European Society for Medical Oncology Immuno-Oncology Congress (ESMO-IO) 2021. These results demonstrated good tolerability, clear evidence of target engagement and pathway inhibition and early but promising signs of activity in combination with chemotherapy and pembrolizumab.

In November 2021, Surface presented scientific posters at the Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper) 2021 Annual Meeting, highlighting SRF617’s potent CD39 inhibition and its effect on promoting pro-inflammatory therapeutic activity in preclinical models.

Additionally, the company presented translational data on IL-27 expression by macrophages in the tumor microenvironment from patients with therapy-resistant non-small-cell lung cancer, supporting continued development of SRF388.
On March 1, 2022, the company granted non-qualified stock options to two new employees to purchase an aggregate of 98,000 shares of the company’s common stock with a per share exercise price of $3.64. The option grants, made under Surface’s 2021 Inducement Plan (the Plan), were granted as an inducement material to the employees entering into employment with the company in accordance with Nasdaq Listing Rule 5635(c)(4) and were granted pursuant to the terms of the Plan.
Selected Anticipated Near-term Corporate Milestones:

Surface will present new translational data on SRF388 at the American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting in April 2022. In addition, the company anticipates presenting updated clinical data from SRF388 in the second quarter of 2022.
Clinical data update for SRF617 is expected in the second half of 2022.
Financial Results:

As of December 31, 2021, cash, cash equivalents and marketable securities were $154.1 million, compared to $175.1 million on December 31, 2020.

Revenue recognized in the fourth quarter ended December 31, 2021, was $0.2 million, compared to revenue of $87.6 million for the same period in 2020. The decrease was a result of the $85 million upfront payment received in the fourth quarter 2020 from GSK. Revenue recognized in the full year ended December 31, 2021, was $2.7 million, compared to $126.2 million for the same period in 2020. The decrease was a result of the $85 million upfront payment received in the fourth quarter 2020 from GSK, as well as the expiration of the final Novartis option purchase period in January 2020 and the corresponding recognition of the remaining deferred revenue under the agreement.

Research and development (R&D) expenses were $16.3 million for the fourth quarter ended December 31, 2021, compared to $10.7 million for the same period in 2020. R&D expenses were $53.6 million for the full year ended December 31, 2021, compared to $41.0 million for the same period in 2020. This increase was primarily driven by continued enrollment and advancement into the expansion stages of our ongoing SRF617 and SRF388 Phase 1 clinical trials. R&D expenses included $2.4 million in stock-based compensation expense for the full year ended December 31, 2021.

General and administrative (G&A) expenses were $7.2 million for the fourth quarter ended December 31, 2021, compared to $8.9 million for the same period in 2020. G&A expenses were $25.1 million for the full year ended December 31, 2021, compared to $23.6 million for the same period in 2020. The decrease in the fourth quarter ended December 31, 2021, was primarily due to increased consulting costs related to the GSK agreement and higher performance bonus achievement in 2020. The increase for the full year ended December 31, 2021, was primarily due to increased salary, recruiting and stock compensation expense associated with an increased headcount in 2021. G&A expenses included $6.1 million in stock-based compensation expense for the full year ended December 31, 2021.

For the fourth quarter ended December 31, 2021, net loss was $24.1 million, or basic and diluted net loss per share of $(0.52). Net income was $67.3 million for the same period in 2020, or basic net income per share of $1.66, and diluted net income per share of $1.56. For the full year ended December 31, 2021, net loss was $78.5 million, or basic and diluted net loss per share of $(1.77). Net income was $59.3 million for the same period in 2020, or basic net income per share of $1.67 and diluted net income per share of $1.57.

Based upon its current operating plan, Surface continues to project cash runway sufficient through 2023.

Redx to Present at the Cowen 42nd Annual Health Care Conference

On March 2, 2022 Redx (AIM: REDX), the clinical-stage biotechnology company focused on discovering and developing novel, small molecule, highly targeted therapeutics for the treatment of cancer and fibrotic disease, reported that Lisa Anson, Chief Executive Officer, and Peter Collum, Chief Financial Officer, will be presenting at the Cowen 42nd Annual Health Care Conference on Wednesday, 9 March 2022 at 15:30 GMT / 10:30 ET (Press release, Redx Pharma, MAR 2, 2022, View Source [SID1234609338]).

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Following the event, a recording will be made available on the investor section of the Company’s website at: View Source

Minomic takes MiCheck® Prostate to ASCO Genitourinary Cancers Symposium in San Francisco

On March 2, 2022 Minomic International Limited reported the Genitourinary Cancers Symposium which was held in San Francisco and presented data from their latest study on the diagnostic test the company has developed to assist in the detection of aggressive prostate cancer (Press release, Minomic, MAR 2, 2022, View Source [SID1234609334]).

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Principal Investigator Dr Neal Shore took attendees through the study: MiCheck Prostate Blood Test for Aggressive Prostate Cancer Designed for the Clinical Lab Setting.

MiCheck Prostate is a patented algorithm that analyses the relative concentration of specific protein biomarkers and one clinical factor, to estimate the risk of a patient having aggressive prostate cancer. It is designed to assist urologists in making more informed decisions when considering a biopsy for their patient.

Dr Shore said: "Clinicians are always desirous for a diagnostic tool that can more accurately detect aggressive prostate cancer, and this optimally identify patients for prostate biopsy."

"For a biomarker test to risk stratify for prostate biopsy decision-making, it should have high sensitivity and clinician friendly implementation."

"This study sought to measure the performance of MiCheck Prostate across multiple platforms."

Minomic CEO Dr Brad Walsh added: "It was great to have Dr Shore present the poster to a US audience ahead of the test becoming available in the country later this year."

"Biopsies are a painful procedure and the wait for a result can cause anxiety both for the patient and their family. It is estimated that about two million American men undergo transrectal biopsies each year to diagnose prostate cancer. About 1-3% of these can lead to sepsis and death, while 250,000 are diagnosed with prostate cancer.

"The US will be a key market for MiCheck Prostate and we will be making announcements on a number of key appointments and initiatives in the coming weeks."