Eiger to Present at Jefferies Virtual Healthcare Conference 2020

On May 26, 2020 Eiger BioPharmaceuticals, Inc. (Nasdaq:EIGR), focused on the development and commercialization of targeted therapies for serious rare and ultra-rare diseases, reported that Eiger management will present a corporate update at the Jefferies Virtual Healthcare Conference on June 4, 2020 from 9:30-9:55 PM ET (Press release, Eiger Biopharmaceuticals, MAY 26, 2020, View Source [SID1234558501]).

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A live webcast of the presentation will be available on the Eiger BioPharmaceuticals website at www.eigerbio.com under the "Investors" tab. A replay of the webcast will be available approximately one hour following the completion of the live event.

Eiger will also host one-on-one meetings with investors as audio conference calls.

A-Alpha Bio Demonstrates Feasibility for Molecular Glue Discovery and Receives Phase II SBIR Funding

On May 28, 2020 A-Alpha Bio reported that it has been awarded a National Science Foundation Phase II Small Business Innovation Research (SBIR) grant to continue developing their AlphaSeq platform for the discovery of molecular glues (Press release, A-Alpha Bio, MAY 26, 2020, View Source [SID1234636940]). AlphaSeq is a proprietary drug discovery platform that applies synthetic biology and next generation sequencing to measure up to millions of protein-protein affinities simultaneously by characterizing all interactions between two protein libraries. A-Alpha Bio’s partners use AlphaSeq for antibody development – for example simultaneously optimizing specificity and cross-reactivity. In addition, AlphaSeq will soon be leveraged for the discovery of protein degrading "molecular glues."

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Molecular glues function by physically sticking two proteins together that would not otherwise interact. More specifically, targeted protein degraders redirect an E3 ubiquitin ligase to bind to a target protein, such as an oncogenic or plaque forming protein, and flag it for degradation. Targeted degradation is an attractive strategy for inhibiting otherwise undruggable proteins and has an enormous potential impact for treating cancers, immunological disorders, and neurodegenerative diseases.

The major barrier to molecular glue discovery is the low probability that a small molecule will "glue" together two particular proteins. Not only must the molecule bind to an E3 ubiquitin ligase, but the presence of the bound small molecule must then redirect binding to a target protein intended for degradation.

"Molecular glue discovery is a really hard problem. The only way to solve it is to test a lot E3 ligase-target interactions," said Randolph Lopez, Co-Founder and CTO of A-Alpha Bio. "With probabilities so low, you have to screen more than you would for a typical small-molecule discovery program – and that’s exactly what AlphaSeq allows us to do."

Using AlphaSeq, A-Alpha Bio measures interactions between an entire library of E3 ubiquitin ligases (humans have over 600) and an entire library of target proteins, instead of just one of each. When a drug candidate is tested, AlphaSeq detects interactions between any ligase–target pair. For example, if 100 ligases and 100 targets are included, a single AlphaSeq assay will measure 10,000 potential interactions, all in less than 1 milliliter of volume. Increasing screening throughput by many orders of magnitude, as AlphaSeq enables, is the type of breakthrough required to discover molecular glues and unlock one of the most promising new drug modalities.

During Phase I of their NSF SBIR award, A-Alpha Bio successfully demonstrated feasibility by expressing E3 ubiquitin ligases and target proteins in their AlphaSeq platform and correctly observing protein interactions that are enhanced by existing molecular glues. With continuing support from an NSF SBIR Phase II award, A-Alpha Bio will construct E3 ligase and target libraries, improve assay sensitivity for the detection of weak protein interactions, and develop a high-throughput screening workflow for molecular glue libraries.

"Targeted protein degradation is one of the most exciting and rapidly growing therapeutic modalities," added Randolph. "We are thrilled to have the National Science Foundation’s continued support to develop AlphaSeq for molecular glue discovery."

CytomX Therapeutics to Host Conference Call and Webcast to Review ASCO ASCO20 Virtual Scientific Program Presentations

On May 26, 2020 CytomX Therapeutics, Inc. (Nasdaq: CTMX), a clinical-stage oncology-focused biopharmaceutical company pioneering a novel class of investigational antibody therapeutics based on its Probody therapeutic technology platform, reported it will host a conference call and audio webcast on Friday, May 29, 2020 from 5:00 p.m. to 6:00 p.m. ET / 2:00 p.m. to 3:00 p.m. PT (Press release, CytomX Therapeutics, MAY 26, 2020, http://ir.cytomx.com/news-releases/news-release-details/cytomx-therapeutics-host-conference-call-and-webcast-review-asco [SID1234558452]). CytomX management will review oral and poster presentations from the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper)’s (ASCO) (Free ASCO Whitepaper) ASCO (Free ASCO Whitepaper)20 Virtual Scientific Program.

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To participate in CytomX Therapeutics’ ASCO (Free ASCO Whitepaper) 2020 Conference Call, please access the call by dialing 1-877-809-6037 (United States) or 1-615-247-0221 (International) referencing Conference ID 4267278. The listen-only audio and slide webcast of the conference call can be accessed under "Events & Presentations" of the Investor Relations section of the Company’s website at View Source Please access the website 15 minutes prior to the start of the call to download and install any necessary audio software. A replay of the webcast will be located under the Investor Relations section of CytomX’s website approximately two hours after the conclusion of the live call and will be available for 30 days following the call.

Alpine Immune Sciences to Participate in Fireside Chat at the Jefferies Virtual Global Healthcare Conference

On May 26, 2020 Alpine Immune Sciences, Inc. (NASDAQ: ALPN), a leading clinical-stage immunotherapy company focused on developing innovative treatments for cancer and autoimmune/inflammatory diseases, reported its participation in an analyst-led fireside chat at the Jefferies Virtual Global Healthcare Conference on Tuesday, June 2, at 10:00 a.m. ET (Press release, Alpine Immune Sciences, MAY 26, 2020, View Source [SID1234558468]).

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A live webcast of the presentation will be available online in the investor relations section of the company’s website at View Source A replay of the presentation will be available on the company website for 90 days following the webcast.

Monte Rosa Therapeutics Discloses $32.5 Million Financing

On May 26, 2020 Monte Rosa Therapeutics, a biotechnology company developing small molecules to degrade disease-related proteins, reported stealth mode revealing a $32.5 million Series A commitment from founding investor Versant Ventures and New Enterprise Associates. Monte Rosa was launched from Ridgeline, Versant’s Discovery Engine based in the Basel Technology Park (Press release, Monte Rosa Therapeutics, MAY 26, 2020, View Source [SID1234558486]). The company is now headquartered in Boston, MA, with research operations in both Boston and Basel, Switzerland.

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Monte Rosa has developed a platform to rationally design small molecules that reprogram ubiquitin ligases to eliminate disease drivers previously deemed undruggable. The platform includes computational capabilities to predict and model ligase-neosubstrate interactions and quantitative proteomics to obtain protein degradation profiles.

Expanding the horizon for cereblon reprogramming

In 2018, Monte Rosa was established in Versant’s Ridgeline laboratories in collaboration with The Institute of Cancer Research (ICR) and Cancer Research UK. Academic co-founders Rajesh Chopra, MD, and Ian Collins, PhD, are prominent leaders in the field of protein degradation.

Nicolas Thomä, PhD, a world-leading chemical and structural biologist at the Friedrich Miescher Institute in Basel, also joined Monte Rosa as scientific advisor. Dr. Thomä recently published a series of seminal papers revealing mechanistic details of cereblon-mediated protein degradation. His work demonstrated the pivotal role of a glycine loop degron on target proteins, and opened up the potential for drug discovery on many more disease-relevant targets. This work underpins Monte Rosa’s platform and approach.

"With our improved understanding of the broad potential of cereblon and other ubiquitin ligases, there is now an opportunity to eliminate major – and currently undruggable – drivers of solid tumors such as transcription factors and adaptor proteins," said Markus Warmuth, MD, CEO of Monte Rosa and a venture partner at Versant.

Developing drug candidates with novel degradation profiles

Monte Rosa has built an integrated drug discovery platform that combines one of the most diverse chemical libraries of protein degraders with in-house proteomics and structural biology capabilities. By the end of 2020, the chemical library is expected to grow to more than 10,000 structures designed for ubiquitin ligase reprogramming.

To date, several validated small molecule leads have been identified through conventional and phenotypic screens along with rational drug design. A number of these leads possess novel degradation profiles and have demonstrated in vivo efficacy across several different tumor models.

"Using this approach we can potentially design drugs for the hundreds to thousands of proteins with glycine loop degrons," said Alex Mayweg, PhD, managing director at Versant and Monte Rosa board member. "Unlike protacs, these small molecules can degrade proteins that lack classical drug-binding pockets, which include known drivers of certain forms of cancer and other serious diseases."

Operating and financing plans

Monte Rosa plans to build out its platform and concurrently develop a portfolio of drug candidates for multiple indications. One of its portfolio leads, MRT-048, has demonstrated a differentiated degradation profile and promising in vivo activity in several models of resistant breast cancer. The molecule is undergoing further preclinical development and safety testing. The company expects to file one or more IND submissions during 2021.

"Monte Rosa has built a formidable drug discovery capability and portfolio based on access to unique insights into ubiquitin ligase reprogramming," said Ali Behbahani, MD, general partner at NEA and Monte Rosa board member. "This approach is now demonstrating the potential to impact patients with intractable forms of cancer."

The company will soon launch a Series B financing to back the development of multiple clinical-stage programs. To capture the full potential of its technology platform, Monte Rosa also will explore discovery-stage pharma collaborations.