Sysmex Receives Approval for a Partial Change to the OncoGuide™ NCC Oncopanel System as a Companion Diagnostic to Futibatinib for Biliary Tract Cancer

On March 15, 2023 Sysmex Corporation (HQ: Kobe, Japan; Chairman and CEO: Hisashi Ietsugu) reported that as of February 28, 2023, Sysmex has received approval for a partial change to its OncoGuide NCC Oncopanel System (the "System") for use as a companion diagnostic to futibatinib (generic name)1 for patients with biliary tract cancer (Press release, Sysmex, MAR 15, 2023, View Source [SID1234628799]).Futibatinib is a molecular-targeted agent currently under development by Taiho Pharmaceutical Co., Ltd. (HQ: Chiyoda-ku, Tokyo, Japan; President and Representative Director: Masayuki Kobayashi).

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Biliary tract cancer is known to develop in approximately 26,000 patients annually in Japan,3 with a 5-year relative survival rate4 of less than 30%,5 and has the second poorest prognosis of any cancer after pancreatic cancer. At present, this disease has few treatment options, and no standard treatment has been sufficiently established for locally advanced or metastatic biliary tract cancer that has progressed after first-line treatment. Development is actively underway in pursuit of molecular-targeted therapeutic agents that target specific genetic abnormalities such as FGFR2 gene6 rearrangements, which are believed to be closely related to cancer cell survival and proliferation.

In 2018, Sysmex became the first manufacturer in Japan to receive manufacturing and marketing approval for a system for use in cancer genome profiling.7 The Company has since contributed to the promotion of cancer genomic medicine in Japan with a testing flow that can be conducted entirely in Japan, while promptly providing the testing to various medical institutions. Sysmex was working on the development of a companion diagnostic device aimed at commercialization, jointly with Taiho Pharmaceutical, which is developing futibatinib, an FGFR inhibitor for the treatment of previously treated locally advanced or metastatic biliary tract cancer harboring FGFR2 gene rearrangements, including gene fusions. On September 2, 2022, Sysmex applied for a partial change with an additional intended use for the System in Japan. Taiho Pharmaceutical applied for manufacturing and marketing approval for futibatinib in Japan on July 28, 2022.

Sysmex has received approval for a partial change to the System to include its use as a companion diagnostic for futibatinib for biliary tract cancer, in addition to cancer genome profiling. This approval will allow the System to be used to detect FGFR2 gene fusions by analyzing gene rearrangements, thereby assisting in identifying patients with biliary tract cancer who may be eligible for futibatinib. Sysmex will press forward with its efforts aimed at early insurance coverage and market introduction in Japan. If this test is available with insurance coverage in the future, it is expected to provide another treatment option for patients with locally advanced or metastatic biliary tract cancer.

Sysmex will continue to work on the early commercialization of high-value testing and diagnostic technologies to offer optimal treatment for each patient, while also contributing to the development and evolution of personalized medicine.

Sporos BioDiscovery to Present Preclinical Findings on SPR1, a Next-Generation TEAD Inhibitor, at the American Association for Cancer Research (AACR) Annual Meeting 2023

On March 15, 2023 Sporos BioDiscovery, Inc. (a wholly owned affiliate of Sporos Bioventures, "Sporos" or the "Company"), a precision oncology company developing a diversified pipeline of small molecule therapeutic programs targeting cancer vulnerabilities in the tumor and tumor microenvironment, reported that it will present a poster highlighting preclinical data from the company’s novel, isoform selective TEAD inhibitor, SPR1, at the American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting 2023 taking place April 14-19, 2023, in Orlando, FL (Press release, Sporos Bioventures, MAR 15, 2023, View Source [SID1234628798]).

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"We look forward to presenting preclinical data on our TEAD inhibitor, which we believe has best-in-class potential based on its optimized TEAD isoform selectivity profile and resultant preclinical activity superior to that of other compounds in development," said Stephen Rubino, Ph.D., Sporos’ Chief Executive Officer. "SPR1 inhibitors show single-agent activity against multiple TEAD-dependent cell lines in vitro and in vivo, including a range of non-NF2 mutation cell lines and those cell lines that are simply YAP-hyperactive. In addition, our differentiated TEAD inhibitors have demonstrated potent synergistic activity in combination with inhibitors of the MAPK pathway, creating the potential for broad applicability across a number of cancers with serious unmet medical need."

Presentation Details:

Title: A next generation TEAD inhibitor with refined isoform specificity for superior safety & efficacy
Session Category: Experimental and Molecular Therapeutics
Session Title: New Drug Targets
Session Date and Time: Sunday Apr 16, 2023, 1:30 PM – 5:00 PM
Abstract Number: 445

RS Research Announces Poster Presentation at the ESMO TAT 2023 Congress

On March 15, 2023 RS Research, a clinical-stage biotechnology start-up developing smart nanomedicines for targeted chemotherapy, reported the acceptance of a poster presentation at the European Society for Medical Oncology Targeted Anticancer Therapies (ESMO TAT) 2023 Congress on 6-8 March in Paris – France, being known as "The Home of Phase I in Oncology" (Press release, RS Research, MAR 15, 2023, View Source [SID1234628797]).

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RS Research’s platform technology allows designing targeted drug candidates for different indications, which yields into development of the company’s own portfolio consisting of 5 drug candidates, as well as an important co-development potential. The nanocarriers introduce a versatile targeting capability and are suitable for loading a single or a combination of chemotherapeutic agents, with superior pharmacokinetic profiles while the targeting enables the drugs to accumulate in the tumor ensuring an enhanced therapeutic index and thus offering reduced toxicity profile.

RS-0139 is the lead candidate in Phase I clinical trial, aiming to deliver docetaxel specifically into integrin receptor expressing tumors such as NSCLC, breast, ovarian, prostate and pancreatic as well as head & neck carcinoma. RS Research Co-Founder and CSO Prof. Dr. Rana Sanyal and Medical Director Gülşah Nomak, MD presented the candidates’ promising preclinical data at ESMO (Free ESMO Whitepaper) TAT 2023.

Poster Title: RS-0139, a novel tumor-targeted delivery of docetaxel, with potent anti-tumor activity in a broad spectrum of tumor cell lines and xenograft models

Date: 6 March 2023

Location: Hall Bordeaux

Poster No: 100P

Presenter: Prof. Rana Sanyal, PhD; Co-Founder & CSO, RS Research | Gülşah Nomak, MD; Medical Director, RS Research

The poster abstract will be available online at the ESMO (Free ESMO Whitepaper) TAT 2023 website.

Protagonist Therapeutics Reports Fourth Quarter and Full Year 2022 Financial Results and Provides Corporate Update

On March 15, 2023 Protagonist Therapeutics (Nasdaq: PTGX) ("Protagonist" or "the Company") reported financial results for the fourth quarter and full year ended December 31, 2022 and provided a corporate update (Press release, Protagonist, MAR 15, 2023, View Source [SID1234628795]).

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"The positive FRONTIER 1 JNJ-2113 (PN-235) data recently reported represents a scientific breakthrough with the potential to transform the treatment landscape for moderate-to-severe plaque psoriasis with oral targeted therapy. We look forward to in-depth presentations of JNJ-2113 pre-clinical and Phase 1 and Phase 2 clinical studies at medical conferences beginning in the second quarter of 2023," said Dinesh V. Patel, Ph.D., President and Chief Executive Officer of Protagonist. "In addition, we are extremely pleased to have announced this morning the positive results from the randomized withdrawal part of the REVIVE study of rusfertide in polycythemia vera (PV). The study met its primary endpoint, with a statistically significant higher number of responders on rusfertide versus placebo (p=0.0003). Improvements in symptoms were observed, and rusfertide was generally well tolerated in the overall study."

Dr. Patel continued, "These positive results from the Phase 2 FRONTIER 1 and REVIVE studies, of JNJ-2113 and rusfertide, respectively, are testaments to the promise of our proprietary platform as well as the expertise, experience and commitment of the Protagonist team. We are focused on enrolling patients globally in the Phase 3 VERIFY study of rusfertide in PV, and we are diligently preparing for the pre-commercial launch-related activities for rusfertide.

"Meanwhile, our discovery engine remains prolific. We are evaluating pre-clinical compounds with the potential to have impact in areas of high unmet medical need, and we are specifically advancing efforts in the oral hepcidin mimetic program. With two assets in late-stage development, Protagonist is now closer than ever to bringing transformative new therapies to patients. As an industry leader in the discovery and development of peptide therapeutics, we hold a unique set of capabilities that position our Company for value creation over the long run," Patel said.

Fourth Quarter 2022 Recent Developments and Upcoming Milestones

Rusfertide: Subcutaneous Injectable Hepcidin Mimetic for Polycythemia Vera (PV) and Other Blood Disorders

· The double-blind, placebo-controlled, 12-week randomized withdrawal portion of the REVIVE study met its primary endpoint, phlebotomy eligibility, with subjects randomized to rusfertide demonstrating a highly statistically significant (p=0.0003) proportion of responders compared to placebo. A study subject was defined as a responder if the subject completed 12 weeks of double-blind treatment while maintaining hematocrit control without phlebotomy eligibility and without phlebotomy. During the 12 weeks of the blinded randomized withdrawal, only 2 of 26 subjects on rusfertide were phlebotomized, keeping 92.3% of patients phlebotomy free in the treatment arm

In patients with moderate or severe Myeloproliferative Neoplasm-Symptom Assessment Form (MPN-SAF) symptom scores at baseline, the change from baseline was statistically significant in fatigue, problems with concentration, inactivity and itching during the 28-week open label Part 1 of the study. Meaningful comparison of symptom assessments in Part 2 are not possible since a majority of subjects randomized to placebo discontinued prior to the 12-week assessment of MPN-SAF symptoms.

· Rusfertide was well tolerated, with localized injection site reactions comprising the majority of reported adverse events. No new safety signals were observed in these data, following presentation of safety data from the REVIVE study at the American Society of Hematology (ASH) (Free ASH Whitepaper) December 2022.

· For PV, Rusfertide has received FDA and EU orphan designation and FDA fast track designation.

JNJ-2113 (formerly PN-235): Oral IL-23 Receptor Antagonist

· The Company announced positive topline results from its collaboration with Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, in the FRONTIER 1 Phase 2b clinical trial evaluating the oral Interleukin-23 receptor (IL-23R) antagonist peptide JNJ-2113 in patients with moderate-to-severe plaque psoriasis.

· Data from the 255-patient study showed that JNJ-2113 achieved the study’s primary efficacy endpoint, with a statistically significant greater proportion of patients who received JNJ-2113 achieving PASI-75 (a 75% improvement in skin lesions as measured by the Psoriasis Area and Severity Index) responses compared to placebo at Week 16 in all five treatment groups. A clear dose response was observed across an eight-fold dose range.

· All treatments were well tolerated, with no meaningful difference in frequency of adverse events across treatment groups versus placebo.

· Data from various pre-clinical and clinical studies on JNJ-2113 will be presented at medical conferences beginning in the second quarter of 2023.

· Phase 1 and preclinical data of JNJ-2113 will be presented on May 12, 2023 at the International Societies for Investigative Dermatology Meeting 2023. More information on this presentation, entitled, "First-in-class oral peptide systemically targeting the IL-23 pathway," is available on the ISID 2023 website at isid2023.org.

Fourth Quarter 2022 Financial Results:

· Cash, Cash Equivalents and Marketable Securities: Cash, cash equivalents and marketable securities as of December 31, 2022 were $237.4 million. The Company expects current cash, cash equivalents and marketable securities to be sufficient to fund its planned operating and capital expenditures through the end of 2024.

· License and Collaboration Revenue: License and collaboration revenue for the fourth quarter and full year 2022 were zero and $26.6 million, respectively, as compared to $8.6 million and $27.4 million for the same periods of 2021. The decreases in revenue from prior year periods were primarily due to a decrease in the level of services the Company provided under the Janssen license and collaboration agreement. The Company completed its performance obligation pursuant to the collaboration as of June 30, 2022.

· Research and Development ("R&D") Expenses: R&D expenses for the fourth quarter and full year 2022 were $29.9 million and $126.2 million respectively, as compared to $38.4 million and $126.0 million, respectively, for the same periods of 2021. The decrease in R&D expenses from prior year quarter was primarily due to lower PN-943 expenses related to the suspension of further program expenditures, a decrease in costs related to the completion of JNJ-2113 and PN-232 Phase 1 trials, and a decrease in research and discovery program expenses.

· General and Administrative ("G&A") Expenses: G&A expenses for the fourth quarter and full year 2022 were $6.6 million and $31.7 million, respectively, as compared to $7.3 million and $27.2 million for the same periods of 2021. The decrease in G&A expenses from prior year quarter was primarily due to a decrease in personnel related expenses during the three months ended December 31, 2022. The increase in G&A expenses from prior year was primarily due to increases in personnel related expenses, including stock-based compensation expense, and other expenses to support Company growth.

· Net Loss: Net loss was $34.2 million, or $0.69 per share, for the fourth quarter of 2022 as compared to a net loss of $36.9 million, or $0.77 per share, for the fourth quarter of 2021. Net loss was $127.4 million, or $2.60 per share, for the full year 2022, as compared to a net loss of $125.6 million, or $2.71, for the full year 2021.

3

PROTAGONIST THERAPEUTICS, INC.
Condensed Consolidated Statements of Operations

(Amounts in thousands except share and per share data)

Three Months Ended Twelve Months Ended
December 31, December 31,
2022 2021 2022 2021
License and collaboration revenue – related party $ — $ 8,617 $ 26,581 $ 27,357
Operating expenses:
Research and development (1) 29,884 38,373 126,215 126,006
General and administrative (1) 6,632 7,260 31,739 27,196
Total operating expenses 36,516 45,633 157,954 153,202
Loss from operations (36,516 ) (37,016 ) (131,373 ) (125,845 )
Interest income 2,251 122 4,060 443
Other income (expense), net 71 (13 ) (80 ) (149 )
Net loss $ (34,194 ) $ (36,907 ) $ (127,393 ) $ (125,551 )
Net loss per share, basic and diluted $ (0.69 ) $ (0.77 ) $ (2.60 ) $ (2.71 )
Weighted-average shares used to compute net loss per share, basic and diluted 49,262,643 48,154,171 49,042,232 46,322,910

(1) Amount includes non-cash stock-based compensation expense.

PROTAGONIST THERAPEUTICS, INC.
Stock-based Compensation

(In thousands)

Three Months Ended Twelve Months Ended
December 31, December 31,
2022 2021 2022 2021
Research and development $ 3,429 $ 2,755 $ 14,719 $ 8,996
General and administrative 2,083 2,269 9,483 7,399
Total stock-based compensation expense $ 5,512 $ 5,024 $ 24,202 $ 16,395

PROTAGONIST THERAPEUTICS, INC.
Selected Consolidated Balance Sheet Data
(In thousands)

December 31, December 31,
2022 2021
Cash, cash equivalents and marketable securities $ 237,355 $ 326,900
Working capital 211,198 298,720
Total assets 247,928 347,695
Deferred revenue-related party — 1,601
Accumulated deficit (536,755 ) (409,362 )
Total stockholders’ equity 215,608 300,021

PTX receives expanded Orphan Drug Designation for all T-cell lymphomas

On March 15, 2023 Prescient Therapeutics (ASX: PTX), reported that it has received an expanded Orphan Drug Designation (ODD) from the Food and Drug Administration (FDA) for its targeted cell therapy PTX-100 that now extends to all T-cell lymphomas (TCLs) (Press release, Prescient Therapeutics, MAR 15, 2023, View Source;utm_medium=rss&utm_campaign=ptx-receives-expanded-orphan-drug-designation-for-all-t-cell-lymphomas [SID1234628794]). This is an encouraging signal from the US regulatory agency, who had already awarded the asset ODD for its potential to treat Peripheral T-cell Lymphoma – and aggressive cancer with an average 5-year survival rate of 32%.

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Prescient had applied for ODD due to the asset’s potential to treat Cutaneous T-cell Lymphoma (CTCL). In a pleasant surprise, the FDA granted the designation broader than PTX’s request. There are over 20 different types of TCL, so this significantly broadens the scope of PTX-100’s potential.

The FDA grants ODD status to drugs and biologics that are intended to treat rare diseases or conditions affecting fewer than 200,000 people in the United States. While drugs with ODD designation still have to go through the same rigorous scientific review process that any other drug must complete for approval or licensing, there is a correlation between receiving the designation and approval: between 2010 and 2016, 75% of all novel cancer drugs that received approval in the United States also qualified as orphan products. During the same time period, the average time between receiving ODD and approval was 5.3 years.

Investors tend to place value in the awarding of an ODD on a therapy. Specifically for smaller biotech companies, the average increase in share price or cumulative abnormal return following an ODD announcement has been found to be 8.87% for nano-caps (

An update on the study, which is being expanded to include up to 12 additional patients with TCL, is due imminently.

The focus of the current expansion cohort are patients with relapsed and refractory TCLs. The company has already achieved a partial response in a patient with aggressive PTCL. The response endured for over 32 months before the disease progressed. Importantly, this response was achieved in a patient that had failed five prior lines of therapy.

At the October 2022 update, one of the patients with CTCL, who had failed four prior lines of therapy, had a very good partial response (VGPR) that had endured beyond 6 months. Visually evident reduction in skin abnormalities were recorded and described by the Principle Investigator of the study, haematologist Professor H. Miles Prince, as "impressive responses". The patient remained on therapy. Two other patients with CTCL that failed three prior lines of therapy have experienced stable disease (SD) that had endured for 4 months. PTX-100 is a first in class compound that blocks an important cancer growth enzyme known as geranylgeranyl transferase-1 (GGT-1). This disrupts oncogenic Ras pathways by inhibiting the activation of Rho, Rac and Ral circuits in cancer cells which leads to apoptosis (death) of the cell. More than 30% of all human cancers, including 95% of pancreatic cancers, 45% of colorectal cancers, 35% of lung cancers and 15% of acute myeloid leukaemia – are driven by mutations of the RAS family of genes.