Araris Biotech AG Announces Research Collaboration with Taiho Pharmaceutical to Develop Next-Generation ADCs Using Araris’ Proprietary Linker-Conjugation Technology

On November 8, 2023 Araris Biotech AG ("Araris"), a Swiss oncology biotech company developing next-generation antibody drug conjugates (ADCs), reported they have entered a collaboration agreement under which Araris will use its proprietary linker-conjugation platform to generate novel ADCs against undisclosed targets provided by Taiho Pharmaceutical Co., Ltd., a Japanese R&D-driven specialty pharma company with a focus on oncology (Press release, Araris Biotech, NOV 8, 2023, View Source [SID1234651282]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

ADCs delivered by Araris will be further tested and evaluated by Taiho. The financial terms of the collaboration agreement were not disclosed.

"We are proud to enter a collaboration with Taiho Pharmaceutical and look forward to working with the Taiho team to develop next-generation ADCs with improved efficacy and tolerability," said Dragan Grabulovski, Ph.D., acting chief executive officer of Araris.

Philipp Spycher, Ph.D., chief scientific officer of Araris added, "This agreement underlines the potential of our linker-payload platform to deliver novel ADCs with excellent properties, and it positions our company as a highly attractive partner for pharmaceutical companies."

Alloy Therapeutics and Wheeler Bio Announce Preferred Service Offering for Alloy Partners to Accelerate the Translation from Discovery to CMC

On November 8th, 2023 Alloy Therapeutics, Inc., a biotechnology ecosystem company and Wheeler Bio, Inc., an agile contract development and manufacturing organization (CDMO), reported the formation of a non-exclusive, preferred service offering to drive translation from Discovery to CMC development and clinical material supply for ecosystem partners (Press release, Alloy Therapeutics, NOV 8, 2023, View Source [SID1234642128]). The organizations are collaborating to provide a premiere service experience for Alloy partners requiring CMC development services from Wheeler as a high-quality, reliable CMC service provider for development and GMP manufacturing.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

Alloy and Wheeler Bio are offering a premium service experience for existing and future ATX-Gx platform users and Alloy Discovery Service partners who also contract Portable CMC development services with Wheeler Bio. This fully integrated offering reflects Alloy’s creative approach to enabling a flexible Insight-to-IND service, connecting partnered antibody projects with Wheeler’s Portable CMC platform to provide a seamless pathway to high quality and affordable lead selection and CGMP material production.

Introducing Wheeler’s Phase offering, where partners of both Alloy and Wheeler will receive the following preferred services:

Dollar-for-dollar reductions in Alloy commercial milestones matching Wheeler Portable CMC services contracted for ‘Lead-to-Tox’ and ‘Lead-to-Clinic’ programs.
Free CMC consulting services to advise ecosystem partners on the translation from discovery to CMC development.
Zero charge CHO pool generation for up to 4 leads, for Alloy partners contracting Wheeler’s Lead-to-Tox or Lead-to-Clinic Portable CMC programs.
50% reduction in initial payment for Alloy partners contracting Wheeler Lead-to-Clinic Portable CMC programs.
Zero reservation fee required to hold manufacturing slots for Alloy partners contracting Wheeler full Lead-to-Clinic Portable CMC programs.
"Following every great antibody and bispecific discovery process, CMC becomes the critical path to treating patients. We developed this preferred offering with Wheeler to support Alloy’s partners with the highest quality cell line development and GMP manufacturing process possible," said Errik Anderson, CEO and Founder at Alloy Therapeutics. "Alloy is helping to lower the cost of drug development by reducing our partners’ downstream payments dollar-for-dollar on their path to the clinic. Wheeler’s high-quality, predictable, fit-for-purpose approach increases the probability of success and reduces the time to clinic for these drug programs. Sharing our economics to help align the ecosystem and accelerate the path of new therapies is a win-win for everyone: Our partners, Alloy, Wheeler, and most importantly, patients."

Alloy is a leading provider of antibody discovery platforms and services with over 150 partners to date with a leading team that has collectively put hundreds of antibodies into the clinic. Alloy’s most popular platform, ATX-Gx, is a best-in-class transgenic mouse strain for fully human antibody discovery which has a proven track record of delivering robust immune response and antibody output with diverse affinity and epitopic coverage. On top of this industry leading humanized transgenic mouse platform Alloy has built a full stack of advanced antibody discovery services including advanced technologies for B-cell repertoire mining and sequencing, proprietary integration of AI/ML, as well as protein engineering and functional testing to rapidly move partners from target idea to validated lead candidate in as quickly as 6 months.

Wheeler Bio’s mission is to solve the translational challenges inherent in advancing from discovery to CMC development and clinical trial material supply. To solve these challenges, Wheeler has developed Portable CMC as an open-source process platform and workflow of pre-clinical and clinical development services based around discrete CMC milestones. The Portable CMC platform is designed to align with clients’ fund-raising milestones, providing a very flexible, affordable, and rapid path to clinical supply. With the implementation of its Portable CMC platform for antibodies, Wheeler Bio is helping emerging biopharma companies reduce manufacturing risks in parallel with drug discovery to enable them to progress smoothly and successfully into drug development and first-in-human studies.

Aligned with its open collaboration model, Alloy partners are still free to use any CDMO of their choice. The preferred service offering is designed to guarantee at least one high-quality CDMO partner for each Alloy partner. By bringing together the ecosystem benefits of Alloy’s world-class discovery engine, along with Wheeler’s reliable CMC services, the Wheeler Phase offering will rapidly traverse the translational gap between discovery and material supply to the clinic. This strategic partnership avoids time lost in selecting a CDMO partner and managing the transition of information to a CDMO that does not know the discovery history, thereby eliminating the CDMO selection process via implementation of a de-risked and proven manufacturing platform (Portable CMC). With implementation of the Phase offering, Wheeler Bio is cementing its unique strategy and commitment to linking discovery and CMC, which most service providers overlook in the path to clinic. This Wheeler CRO partnering model can also be applied more broadly with other discovery providers to further bridge the translational gap between discovery and CMC clinical delivery.

"By closely aligning Alloy’s discovery platform with Wheeler’s development and manufacturing platform, our ecosystem clients benefit immensely by skipping the CDMO RFP process while reducing risk in tech transfers," said Jesse McCool, CEO and Co-Founder at Wheeler. "Our bioprocess models are in lockstep with ATX-Gx derived antibodies, so Wheeler services represent the best, most efficient use of CMC capital for Alloy partners."

"We are elated to participate as an early adopter of the Alloy-Wheeler partnership to speed our path from discovery to CMC development and first patient dosing," stated Hemanta Baruah, Co-Founder and CEO at Aakha Biologics. "Both Alloy and Wheeler are laser focused on meeting our needs as a small biotech start-up with specific goals to generate early data to further enable our fundraising efforts, while also providing a rapid path to the clinic."

Ellis and CStone signed an exclusive commercial promotion agreement for the RET inhibitor Pujihua® (Platinib capsules) in mainland China

On November 8, 2023 Shanghai Alix Pharmaceutical Technology Co., Ltd. ( 688578.SH ) and CStone Pharmaceuticals ( 02616.HK ) signed a commercialization strategic cooperation agreement, and Alix obtained a RET inhibitor Pujihua ( Platinib Capsules) has the exclusive commercial promotion rights in mainland China (Press release, CStone Pharmaceauticals, NOV 8, 2023, https://www.allist.com.cn/newsd/101/2077.html [SID1234642121]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

Focusing on the research, development and commercialization of lung cancer treatment, Ailes has built a mature and experienced marketing team covering more than 1,200 hospitals in core market areas. With excellent sales capabilities, the sales of the core product, the third-generation EGFR-TKI Aversa ( vometinib mesylate tablets), have continued to grow rapidly since it was approved for marketing in 2021 , with revenue of RMB 1.35 billion in the first three quarters of 2023. , an increase of 160.34% compared with the same period last year , achieving a net profit of 410 million yuan. Excellent marketing capabilities have become another core competitiveness of Ellis.

Pujihua is the first RET inhibitor approved for marketing in mainland China. It is used to treat RET gene fusion-positive locally advanced or metastatic non-small cell lung cancer ( NSCLC ) and RET- mutant thyroid medullary disease that have previously received platinum-containing chemotherapy. thyroid cancer ( MTC ) and RET fusion-positive thyroid cancer ( TC ). In June 2023 , the new indication of Pujihua was approved by the China National Medical Products Administration for the first-line treatment of RET gene fusion-positive locally advanced or metastatic non-small cell lung cancer, further expanding the coverage of the patient population. RET fusion is a newly discovered driver gene mutation in lung cancer. RET fusion patients account for about 1-2% of non-small cell lung cancer. There are about 10,000-20,000 new patients in China every year . The commercial cooperation between Ellis and CStone Pharmaceuticals will give full play to the strong sales capabilities of Ellis in the field of lung cancer treatment and the product advantages of Pujihua , expand the market coverage of Pujihua , benefit more patients, and provide Both companies have achieved performance growth.

Regarding this cooperation, Alex Vice Chairman Hu Jie said : "Alice is very pleased to reach a commercialization cooperation with CStone Pharmaceuticals for Pujihua , which will definitely benefit the win-win growth of both companies. Ellis is committed to To provide the best treatment options for cancer patients, while successfully independently developing and obtaining the approval of Aifusa , we have also created a commercialization team with a wide coverage that focuses on the field of lung cancer and has professional academic promotion capabilities. Aifusa is now on the market. Since then, the sales performance has been remarkable. Pujihua is a highly selective RET inhibitor that has been approved for multiple indications in many countries and regions around the world, including China and the United States, with remarkable efficacy and good safety. The cooperation is highly in line with the development strategy and resources of Ellis, and will further expand the coverage of Ellis in the field of lung cancer, give full play to its marketing advantages, and rapidly increase the sales of Pujihua in mainland China, so that more patients can benefit from it. CStone is an outstanding company focused on the research and development of innovative tumor immunotherapy and precision treatment drugs. We look forward to establishing more extensive cooperation with CStone in more product pipelines and scientific research fields."

Dr. Yang Jianxin, CEO of CStone Pharmaceuticals, said: "We are very pleased to reach this cooperation with Ellis, which will undoubtedly maximize the market value of Pujihua in mainland China. As the first RET inhibitor approved for marketing in mainland China, As an agent, Pujihua has benefited thousands of patients with non-small cell lung cancer and thyroid cancer, and has the potential to further expand in many other indications. We firmly believe that Alys has strong commercialization capabilities in the field of precision treatment of lung cancer. and promotion experience will be deeply integrated with the huge clinical value of Pujihua , helping Pujihua benefit more Chinese patients. At the same time, we also look forward to both parties giving full play to their respective pipeline advantages to further promote more drug research and development, clinical development, etc. potential cooperation to jointly bring more high-quality innovative treatments to Chinese patients."

About Pujihua ( Platinib Capsules)

Pujihua is an oral, once-daily, potent and highly selective RET inhibitor . The China National Medical Products Administration has approved Pujihua for the treatment of adult patients with RET gene fusion-positive locally advanced or metastatic non-small cell lung cancer, adults with advanced or metastatic RET-mutated medullary thyroid cancer who require systemic therapy , and Pediatric patients 12 years and older, and adults and pediatric patients 12 years and older with advanced or metastatic RET fusion-positive thyroid cancer who require systemic therapy and are refractory to radioactive iodine (if radioactive iodine is applicable) .

Pujihua has been approved in Hong Kong, China, for the treatment of adult patients with RET gene fusion-positive metastatic non-small cell lung cancer, and in Taiwan, China, for the treatment of locally advanced or metastatic RET fusion-positive non-small cell lung cancer. Adult patients with advanced or metastatic RET -mutated MTC who require systemic therapy and advanced or metastatic RET fusion-positive thyroid cancer who require systemic therapy and are refractory to radioactive iodine therapy (if radioactive iodine therapy is applicable) .

The U.S. Food and Drug Administration has approved it to be marketed under the trade name GAVRETO . The indications are: for the treatment of adult patients with metastatic RET fusion-positive non-small cell lung cancer confirmed by FDA- approved testing methods and who require systemic therapy. Adults and pediatric patients 12 years and older with advanced or metastatic RET fusion-positive thyroid cancer that is refractory to radioactive iodine (if applicable) . The thyroid cancer indication was approved under the accelerated approval pathway based on objective response rate ( ORR ) and duration of response ( DOR ) data. Continued approval for these indications may depend on verification and description of clinical benefit in confirmatory trials. The European Commission has granted conditional marketing authorization to GAVRETO as a monotherapy for the treatment of adult patients with RET fusion-positive advanced non-small cell lung cancer who have not received prior treatment with a RET inhibitor.

About RET fusion-positive non-small cell lung cancer

The incidence of lung cancer has continued to increase in China in recent years. According to the latest global cancer burden data for 2020 released by the World Health Organization’s International Agency for Research on Cancer (IARC), there will be approximately 820,000 new lung cancer cases and approximately 710,000 deaths from lung cancer in China in 2020 . Lung cancer is the leading cause of cancer-related death among both men and women with cancer. Among them, non-small cell lung cancer accounts for the majority of lung cancers.

In the field of lung cancer, driver gene mutations such as EGFR , ALK , and ROS1 have become widespread, and targeted drugs targeting these driver genes have been approved for marketing. RET fusion is a newly discovered lung cancer driver gene. RET fusion patients account for about 1-2% of non-small cell lung cancer and are common in young people who do not smoke.

About RET variant thyroid cancer

Thyroid cancer is the most common endocrine malignant tumor, and its incidence has increased significantly in recent years. According to the latest global cancer burden data for 2020 released by the World Health Organization’s International Agency for Research on Cancer (IARC), there will be approximately 220,000 new cases of thyroid cancer in China in 2020 , including approximately 170,000 new cases in women . The incidence rate of thyroid cancer ranks fourth among all malignant tumors among women in urban areas of China .

Thyroid cancer is clinically divided into multiple subtypes such as papillary carcinoma, follicular carcinoma, anaplastic carcinoma, and medullary carcinoma. Different types of thyroid cancer have different treatment methods and prognosis based on their tumor characteristics.

RET fusions and activating mutations are key disease drivers in many cancer types, including non-small cell lung cancer and multiple types of thyroid cancer. About 10-20% of patients with papillary thyroid cancer (the most common type of thyroid cancer) carry RET fusions, and about 90% of patients with advanced medullary thyroid cancer (about 2-5% of thyroid cancers ) carry RET mutations.

Erasca to Present at Upcoming Investor Conferences in November

On November 8, 2023 Erasca, Inc. (Nasdaq: ERAS), a clinical-stage precision oncology company singularly focused on discovering, developing, and commercializing therapies for patients with RAS/MAPK pathway-driven cancer, reported that management will participate in the following investor conferences in November 2023. Management will also participate in one-on-one investor meetings (Press release, Erasca, NOV 8, 2023, View Source [SID1234639352]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

Jefferies London Healthcare Conference (November 14 – 16, 2023)
Location: Waldorf Hilton, London, UK
Format: Fireside Chat
Date and Time: Wednesday, November 15, 2:30-2:55 PM GMT
Webcast: View Source

6th Annual Evercore ISI HealthCONx Conference (November 28 – 30, 2023)
Location: Kimpton Epic Hotel, Miami, FL
Format: Fireside Chat
Date and Time: Tuesday, November 28, 11:15-11:35 AM ET
Webcast: View Source

An archived replay of the events will be available for 30 days following the webcast at Erasca.com/events.

Assertio Reports Third Quarter 2023 Financial Results

On November 8, 2023 Assertio Holdings, Inc. ("Assertio" or the "Company") (Nasdaq: ASRT), a specialty pharmaceutical company that acquires, commercializes and develops safe and effective therapies that make a difference in the lives of patients, reported financial results for the third quarter ended September 30, 2023 (Press release, Assertio Holdings, NOV 8, 2023, View Source [SID1234639223]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

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

                  Schedule Your 30 min Free Demo!

"Our third quarter results were disappointing, with the loss of Indocin exclusivity and Rolvedon results below expectations driving significant charges to our net income. While we are learning that certain aspects of the acquisition may not be everything we initially expected, we did not buy Spectrum just for the third quarter. The addition of Rolvedon diversifies and extends our portfolio’s duration, plus brings improved commercial access and business-to-business contracting teams that are important to our strategic direction," said Dan Peisert, CEO of Assertio. "We have taken immediate steps to improve the business and remain committed to building a strategic path for Rolvedon’s long-term sustainable growth."

"Despite these headwinds, Assertio’s innovative non-personal platform continues to drive profitable growth on our other assets. Sympazan achieved another new monthly high on a 4% increase in total prescription volume quarter over quarter, and new payor coverage drove volumes and Net Product Sales for Otrexup up 4% and 6%, respectively, for the nine months year-to-date," said Peisert. "We have built this platform to scale and accommodate assets across a variety of therapeutic categories as we continue to pursue additional licensing and acquisition opportunities that can leverage these capabilities, bringing further value to Assertio and capitalizing on our existing liquidity."