Viracta Therapeutics to be Added to the Nasdaq Biotechnology Index

On December 16, 2021 Viracta Therapeutics, Inc. (Nasdaq: VIRX), a precision oncology company targeting virus-associated malignancies, reported that it has been selected for addition to the Nasdaq Biotechnology Index (Nasdaq: NBI), effective prior to market open on Monday, December 20, 2021 (Press release, Viracta Therapeutics, DEC 16, 2021, View Source [SID1234597312]).

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The NBI is designed to track the performance of a set of securities listed on The Nasdaq Stock Market (Nasdaq) that are classified as either biotechnology or pharmaceutical according to the Industry Classification Benchmark (ICB). The NBI is re-ranked each year and is calculated under a modified capitalization-weighted methodology. Additionally, the NBI forms the basis for a number of Exchange Traded Funds (ETFs). More information about the NBI, including eligibility criteria, can be found at View Source

Targovax ASA: Primary insiders share purchase

On December 16, 2021 Targovax and primary insider,reported that it has on 16 December 2021 purchased 50,000 shares in Targovax ASA ("the Company") at an average share price of NOK 2.137 per share (Press release, Targovax, DEC 16, 2021, View Source [SID1234597310]).

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Following this transaction, Ola Melin and his close associates holds 50,000 shares and 250,000 share options in the Company.

Please see the attached notification of trade for further information.

PureTech Provides End of Year Report on Key Progress Across Wholly Owned Programs and Founded Entities

On December 16, 2021 PureTech Health plc (Nasdaq: PRTC, LSE: PRTC) ("PureTech" or the "Company"), a clinical-stage biotherapeutics company dedicated to discovering, developing and commercializing highly differentiated medicines for devastating diseases, reported on the key progress made across its Wholly Owned Programs1 and Founded Entities2 in 2021, including some updates that were not previously reported (Press release, PureTech Health, DEC 16, 2021, View Source [SID1234597309]).

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Daphne Zohar, Founder and Chief Executive Officer of PureTech, commented: "2021 has been a year of profound achievements and fundamental growth across our Wholly Owned Programs and our Founded Entities. With the support of our shareholders, we have pioneered a unique R&D model that has been successful in identifying, inventing and advancing novel therapeutic candidates for serious diseases and creating wholly-owned programs as well as both public and private Founded Entities with substantial value. We are proud of our execution and successes and are excited about using that strong foundation to catalyze value as we enter into an important, milestone-rich 2022, having the benefit of a strong balance sheet from which to drive value."

PureTech’s Wholly Owned Programs are comprised of six therapeutic candidates and four lymphatic and inflammation platforms. Additionally, PureTech’s Founded Entities are advancing 19 therapeutics and therapeutic candidates, of which two have been cleared for marketing by the U.S. Food and Drug Administration (FDA) and granted marketing authorization in the European Economic Area, and 14 are clinical stage. Key highlights include the following:

Wholly Owned Programs

· LYT-100 (deupirfenidone), in development for potential treatment of conditions involving inflammation and fibrosis:

o Progressed Phase 2 clinical trial in patients with Long COVID respiratory complications. Enrollment is expected to be completed by the end of 2021, with topline results anticipated in the first half of 2022.

o Progressed Phase 2a clinical trial in patients with breast cancer-related, upper limb secondary lymphedema. Results are anticipated in 2022.

o Presented the results of the Phase 1 multiple ascending dose and food effect study of LYT-100 at the virtual European Respiratory Society (ERS) International Congress. The results from the study were subsequently published in the journal Clinical Pharmacology in Drug Development.

o PureTech plans to provide further details around its development plans for LYT-100 in additional inflammatory and fibrotic conditions, such as idiopathic pulmonary fibrosis, myocardial fibrosis and other organ system fibrosis.

· LYT-200 (anti-galectin-9 mAb) & LYT-210 (anti-gamma delta-1 mAb), in development for the potential treatment of a range of cancer indications:

o LYT-200 was granted orphan drug designation by the U.S. FDA for the treatment of pancreatic cancer.

o Progressed Phase 1/2 trial of LYT-200 for the potential treatment of a range of solid tumors. Results from the Phase 1 portion are anticipated in the first half of 2022.

o Entered into a clinical trial and supply agreement with BeiGene to evaluate LYT-200 in combination with tislelizumab in solid tumors.

o Presented new research at the American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting demonstrating that LYT-210 is both highly specific and highly potent, rapidly inducing cell death of immune-suppressive γδ1 T cells, while sparing other T cells that play important roles in a healthy immune response. The research was conducted using both patient blood and cancer tissue.

· LYT-300 (oral allopregnanolone), in development for the potential treatment of neurological and neuropsychological conditions, & Glyph Technology Platform:

o Initiated a Phase 1 clinical study in healthy volunteers to evaluate safety, tolerability, and pharmacokinetic profile, as well as explore the impact of LYT-300 on b-EEG, a marker of GABAA target engagement, thus potentially providing early insights into the mechanistic effects of LYT-300. Results from the study will inform the design of possible future studies in indications that could include depression, anxiety, sleep disorders, fragile X tremor-associated syndrome, essential tremor and epileptic disorders, among others.

o Presented preclinical proof-of-concept data at the American College of Neuropsychopharmacology (ACNP) Annual Meeting showing that systemic exposure of natural allopregnanolone was achieved after oral administration of LYT-300 in multiple preclinical animal models.

o Published preclinical proof-of-concept work in Nature Metabolism and the Journal of Controlled Release supporting the Glyph technology platform’s ability to directly target the lymphatic system with a variety of therapies.

· LYT-500 (oral IL-22 + anti-inflammatory), in development for the potential treatment of inflammatory bowel disease, LYT-503 (partnered non-opioid pain program), in development for the potential treatment of interstitial cystitis/bladder pain syndrome, & Alivio Technology Platform:

o Declared LYT-500 therapeutic candidate. Progressed preclinical proof-of-concept work.

o Advancing LYT-503 as a potential targeted non-opioid treatment for interstitial cystitis or bladder pain syndrome in collaboration with a partner, following the exercise of a license option under an existing research and development collaboration. An Investigational New Drug Application is planned to be filed in 2022.

o Evaluating other potential therapeutic candidates leveraging Alivio technology platform for Wholly Owned Pipeline expansion.

· Orasome Technology Platform:

o Established preclinical proof-of-concept supporting the platform’s potential to achieve therapeutic levels of proteins in circulation following the oral administration of therapeutic protein expression systems. PureTech intends to generate additional preclinical data in 2022. Using the Orasome technology platform, it may be possible for a patient to take an oral drug product that will permit their own gastrointestinal tract cells to make virtually any type of therapeutic protein. This approach also has the potential to provide a more convenient and significantly less expensive means to administer biological medicines.

· Meningeal Lymphatics Program:

o Published preclinical research in Nature suggesting that restoring lymphatic flow in the brain has the potential to address a range of neurodegenerative diseases, such as Alzheimer’s and Parkinson’s diseases and associated neuroinflammation. The work also uncovered a link between dysfunctional meningeal lymphatics and damaging microglia activation in Alzheimer’s disease, suggesting another route by which restoring healthy drainage patterns could improve clinical outcomes.

Founded Entities:

· Gelesis

o Broadly launching Plenity, an FDA-cleared weight management approach, in the U.S. to adults who meet the prescription criteria. Gelesis’ first commercial-scale manufacturing line at the facility is also now complete and validated.

o Achieved both primary endpoints in LIGHT-UP study of GS200 in adults with overweight or obesity who also have prediabetes or type 2 diabetes. Gelesis continues to analyze these data as it plans its next steps in the development of GS200 and plans to present the detailed results in a scientific venue.

o Initiated Phase 2 study of GS300, which is in development for the potential treatment of nonalcoholic fatty liver disease/non-alcoholic steatohepatitis (NAFLD/NASH).

o Entered into definitive business combination agreement with Capstar Special Purpose Acquisition Corp. Upon completion of the transaction, the combined company’s securities are expected to be traded on the New York Stock Exchange (NYSE) under the symbol "GLS".

· Akili

o Completed a $160 million financing, a new licensing agreement with Australian digital health company, TALi, and new gaming features and functionalities for EndeavorRx.

o Initiated Phase 2 study of AKL-T01 for COVID brain fog in collaboration with Weill Cornell and Vanderbilt.

o Published full data in Nature Digital Medicine from STARS Adjunct study, which evaluated impact of EndeavorRx (AKL-T01) on symptoms and functional impairments in children with attention-deficit/hyperactivity disorder (ADHD).

o Announced results from Shionogi’s Phase 2 study of SDT-001 (Japanese version of AKL-T01) that showed treatment was well-received by patients and demonstrated improvements in ADHD inattention symptoms consistent with those seen across previous studies of AKL-T01.

· Karuna

o Announced all four Phase 3 trials in the EMERGENT program, the clinical program evaluating KarXT (xanomeline-trospium) for the treatment of psychosis in adults with schizophrenia, are enrolling. Karuna anticipates reporting topline data from the Phase 3 EMERGENT-2 trial in mid-2022 and from the Phase 3 EMERGENT-3 trial in the second half of 2022.

o Initiated the Phase 3 ARISE trial evaluating KarXT for the treatment of schizophrenia in adults who experience an inadequate response to current standard of care.

o Reported data from completed Phase 1b trial evaluating safety and tolerability of KarXT in healthy elderly volunteers. Karuna plans to initiate a Phase 3 program evaluating KarXT for the treatment of psychosis in Alzheimer’s disease in mid-2022.

o Published results from the Phase 2 EMERGENT-1 clinical trial evaluating KarXT for the treatment of schizophrenia in the New England Journal of Medicine (NEJM).

o Announced entry into an exclusive license agreement with Zai Lab for the development, manufacturing and commercialization of KarXT in Greater China, including mainland China, Hong Kong, Macau, and Taiwan.

· Vor

o Completed initial public offering on Nasdaq under ticker symbol "VOR".

o Initiated a Phase 1/2a trial of VOR33 in acute myeloid leukemia (AML).

o Granted Fast Track designation by the FDA for VOR33.

o Entered into collaboration with Janssen Biotech, Inc. (Janssen), to investigate the combination of Vor’s "invisible" eHSC transplant platform with one of Janssen’s bi-specific antibodies in development for AML.

· Follica

o Announced the appointment of two leaders in aesthetic medicine and dermatology to its Board of Directors, Tom Wiggans, former CEO of Dermira, and Michael Davin, former CEO of Cynosure.

o Continued to advance regenerative biology platform, including preparing for a Phase 3 registration program in male androgenetic alopecia, which is expected to be initiated in 2022.

· Vedanta

o Achieved primary endpoint in Phase 2 clinical trial of VE303, an orally administered investigational live biotherapeutic product (LBP) in development for the prevention of recurrent C. difficile infection (CDI) in high-risk patients.

o Completed a $68 million financing, which included a $25 million investment from Pfizer as part of the Pfizer Breakthrough Growth Initiative.

· Sonde

o Launched Sonde Mental Fitness, a voice-enabled mental health detection and monitoring technology that uses a brief voice journal entry to evaluate mental well-being, expanding Sonde beyond respiratory health.

o Announced strategic collaboration with Qualcomm Technologies to embed Sonde vocal biomarker technology into its latest Snapdragon mobile chipsets to provide smartphone OEMs with native, voice-enabled health tracking capabilities.

· Entrega

o Continued advancement of ENT-100 platform for the oral administration of biologics, vaccines and other drugs that are otherwise not efficiently absorbed when taken orally.

o Continued collaboration with Eli Lilly to investigate the application of the Entrega peptide administration technology to certain Eli Lilly therapeutic candidates.

1) References to "Wholly Owned Programs" refer to the Company’s six therapeutic candidates (LYT-100, LYT-200, LYT-210, LYT-300, LYT-500 and LYT-503/IMB-150), four lymphatic and inflammation platforms and potential future therapeutic candidates and platforms that the Company may develop or obtain. References to "Wholly Owned Pipeline" refer to LYT-100, LYT-200, LYT-210, LYT-300, LYT-500 and LYT-503/IMB-150. On July 23, 2021, Imbrium Therapeutics exercised its option to license LYT-503/IMB-150 pursuant to which it is responsible for all future development activities and funding for LYT-503/IMB-150.

2) Founded Entities represent companies founded by PureTech in which PureTech maintains ownership of an equity interest and, in certain cases, is eligible to receive sublicense income and royalties on product sales. As of June 30, 2021, PureTech maintained control over Follica Incorporated, Vedanta Biosciences, Inc., Sonde Health, Inc. and Entrega, Inc. by virtue of (a) majority voting control or (b) the right to elect representation to the entity’s Board of Directors. As of June 30, 2021, PureTech did not have a controlling interest in Gelesis, Inc., Karuna Therapeutics, Inc., Akili Interactive Labs, Inc. and Vor Biopharma Inc.

Notable Presents Clinical Validation Data from Two Phase 2 Trials in Adult and Pediatric Acute Myelogenous Leukemia at the 63rd American Society of Hematology (ASH) Annual Meeting

On December 16, 2021 Notable Labs, Inc. (Notable), a clinical-stage platform therapeutics company, reported that results from two ongoing Phase 2 clinical trials examining the performance of its high-fidelity predictive precision medicines platform in predicting clinical outcomes in acute myelogenous leukemia (AML) standard-of-care settings (Press release, Notable Labs, DEC 16, 2021, View Source [SID1234597308]). These data were recently presented at the 63rd American Society of Hematology (ASH) (Free ASH Whitepaper) Annual Meeting and Exposition.

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Data from the first clinical trial were presented in a poster entitled "Ex Vivo Drug Sensitivity Assay Correlates with Clinical Response and Identifies Panobinostat and Bortezomib as a Potential Novel Drug Combination for Pediatric AML". In a trial conducted at Texas Children’s Hospital, pediatric and young adult de novo AML patients were treated with ADE (Cytarabine, Daunorubicin, Etoposide) alone or in combination with Atovaquone. Peripheral blood or bone marrow samples obtained prior to treatment (n=13) were assessed on Notable’s ex vivo predictive precision medicines platform for responsiveness to ADE. No treatment decisions were made based on these results. Importantly, ex vivo response prediction scores correlated with both minimal residual disease (MRD; r=0.63) and 1-year relapse-free survival (RFS; r=0.59) in this AML population. Moreoever, the Notable predictive score accurately separated responders and non-responders using a MRD threshold of 1%, suggesting that pre-selection of predicted responders using Notable’s platform could potentially identify pediatric AML patients who were likely to respond to standard induction therapy and prevent unnecessary toxicity and delay to more efficacious treatment for treatment non-responsive patients.

Data from the second clinical trial were presented in a poster entitled "Prediction of Clinical Response to Venetoclax Plus Decitabine in AML Using a 7-Day Ex Vivo Assay". In this ongoing Phase 2 trial, currently being conducted at MD Anderson Cancer Center, unfit de novo or relapsed/refractory AML patients are being treated with venetoclax combined with decitabine. In order to determine the utility of Notable’s precision medicines platform in predicting responding patients in this clinical setting, peripheral blood samples obtained prior to treatment were assessed for ex vivo responsiveness to venetoclax plus decitabine. In the initial group of patients, Notable’s predicitive platform correctly identified 5 out of 6 patients demonstrating significant response to this treatment (CR + CRi), suggesting that pre-selection of patients using Notable’s platform could lead to enhanced response rates in adult unfit and relapsed/refractory AML patients eligible for venetoclax plus decitabine.

"These two clinical studies provide further validation of Notable’s predictive precision medicines platform in standard of care settings. These exciting data advance our mission to design and deliver predictive precision medicines by matching treatments with precisely the patients who clinically respond to them," says Joe Wagner, PhD, Chief Scientific Officer of Notable.

"The ability to accurately predict clinical response is especially meaningful for pediatric patients with life-threatening conditions, and progress on this front is important for our patients," says Alexandra Stevens, Assistant Professor, Section of Hematology-Oncology at Texas Children’s Hospital. "Accurate predictive precision medicine will spare children from receiving treatments that are likely to be ineffective for them and thus from exposure to unnecessary toxicity."

The meeting was held virtually and in person in Atlanta, GA, from December 11-14, 2021.

The posters are available for viewing on Notable’s website: View Source

For more details about the ASH (Free ASH Whitepaper) Annual Meeting please visit: View Source

Nkarta Receives U.S. FDA Orphan Drug Designation for NKX101 for Treatment of Patients with AML

On December 16, 2021 Nkarta, Inc. (Nasdaq: NKTX), a clinical-stage biopharmaceutical company developing engineered natural killer (NK) cell therapies to treat cancer, reported that the U.S. Food and Drug Administration (FDA) has granted orphan drug designation (ODD) to NKX101 for treatment of acute myeloid leukemia (AML) (Press release, Nkarta, DEC 16, 2021, View Source [SID1234597307]).

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NKX101 is a novel investigational NK cell therapy, engineered to augment the innate anti-tumor biology of NKG2D. NKG2D is an activating receptor found on naturally occurring NK cells that triggers the targeted killing of stressed and cancerous cells.

AML is a blood cancer that disrupts the production of normal blood cells in the bone marrow. In patients with AML, the five-year survival rate is 26%. While frontline therapy induces remission, most patients will relapse within 3 years. No standard of care is currently available for patients with relapsed/refractory (r/r) AML. These patients may be treated with various chemotherapeutic approaches, all of which have poor results. Clinical trials have resulted in complete response rates of 12% to 18% and a 3 to 9 month median overall survival in this challenging population.

"This orphan drug designation acknowledges the urgent need for new treatment options for patients with AML," said Kanya Rajangam, MD, PhD, Chief Medical Officer of Nkarta. "At Nkarta, we are committed to advancing our NK cell therapy platform to develop ground-breaking treatment options for cancer, and we look forward to working with the leukemia community and the FDA to deliver the unique benefits of off-the-shelf cell therapy to AML patients."

NKX101 is currently being studied in a first-in-human Phase 1 clinical trial in adults with r/r AML or myelodysplastic syndrome (MDS). As previously announced, Nkarta expects to announce initial data from the NKX101 clinical trial in the first half of 2022.

The FDA grants ODD to drugs defined as those intended for the treatment, diagnosis or prevention of rare diseases that affect fewer than 200,000 people in the United States. ODD may qualify the company developing the drug for certain development incentives, including tax credits for qualified clinical testing, prescription drug user fee exemptions and seven-year marketing exclusivity upon FDA approval.

About NKX101
NKX101 is an investigational, off-the-shelf cancer immunotherapy that uses natural killer (NK) cells derived from the peripheral blood of healthy donors and engineered with membrane-bound IL-15 and a chimeric antigen receptor (CAR) targeting NKG2D ligands on tumor cells. NKG2D, a key activating receptor found on naturally occurring NK cells, induces a cell-killing immune response through the detection of stress ligands that are widely expressed on cancer cells. By engineering NKX101 with the proprietary NKG2D-based CAR, the ability of NK cells to recognize and kill tumor cells in pre-clinical models is increased significantly compared to non-engineered NK cells. The addition of membrane-bound IL15, a proprietary version of a cytokine for activating NK cell growth, has been shown in pre-clinical models to enhance the proliferation, persistence and sustained activity of NK cells. To learn more about the NKX101 clinical trial in adults with AML or MDS, please visit ClinicalTrials.gov.