Adimab Provides 2021 Update on Clinical Pipeline

On January 19, 2022 Adimab, LLC, the global leader in the discovery and optimization of fully human monoclonal and bispecific antibodies, reported that 12 new partner programs entered clinical development in 2021, including programs by Biotheus, Dragonfly, IASO, Iconic, Innovent, Mapp Biopharmaceutical, and Surface Oncology (Press release, Adimab, 19 19, 2022, View Source [SID1234605662]). This brings the total number of Adimab partner programs that have entered the clinic to 55.

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The most advanced program from Adimab’s platform is Tyvyt (Sintilimab), currently marketed in China by Innovent and Lilly. In 2021, Innovent and Lilly filed a BLA with the FDA for approval in the United States.

There are currently six additional programs in pivotal trials.

"It’s been exciting to see so many of our partners’ programs advance into the clinic. Over the last four years alone we have seen 45 new programs enter clinical trials. In addition to the volume, the success these programs are having in the clinic is remarkable," said Guy Van Meter, Chief Business Officer of Adimab.

In 2021, Adimab partners exercised 10 commercial licenses to advance programs into development, bringing the total number of optioned programs to more than 85. Partners exercising commercial options in 2021 include Biotheus, Bristol Myers Squibb, IGM Biosciences, Immunitas Therapeutics, Mapp Biopharmaceutical, Regeneron, Sanofi, and Therini, among others.

"Our goal has always been long term value creation and alignment with our partners – we win when they win. This philosophy has focused the organization on quality and ultimately enabling clinical success for our partners. Today’s announcement highlights how well we are doing against this important metric," said Tillman Gerngross, Chief Executive Officer and Co-Founder of Adimab.

Panavance Announces Abstract and Poster at ASCO Gastrointestinal Cancers Symposium, Providing an Update on the Status of GP-2250 Clinical Trial in Pancreatic Cancer Patients

On January 19, 2022 Panavance Therapeutics Inc. ("Panavance") reported an abstract and poster at ASCO (Free ASCO Whitepaper) Gastrointestinal Cancers Symposium, January 20-22, 2022, in San Francisco, "A Phase 1/2 study to evaluate the safety, tolerability, and preliminary efficacy of GP-2250 in combination with gemcitabine for advanced or metastatic pancreatic adenocarcinoma," (authors: Dr. Anup Kasi and Dr. José Iglesias, Poster TPS620) (Press release, Panavance Therapeutics, JAN 19, 2022, View Source [SID1234605663]). The open-label trial for patients with advanced/metastatic pancreatic cancer who were previously treated with FOLFIRINOX is evaluating the safety and tolerability of escalating doses of GP-2250 together with gemcitabine.

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GP-2250 is a broadly active, tumor cell selective, small molecular weight, metabolic enzyme inhibitor with a first-in-class mechanism of action that limits aerobic glycolysis and Krebs cycle by inhibiting GAPDH, alpha-ketoglutarate dehydrogenase, pyruvate dehydrogenase, and the tumor promotor NFkB. In preclinical research, it suppresses cancer cells largely by disrupting their energy metabolism—bringing about cancer cell death.

The ASCO (Free ASCO Whitepaper) Gastrointestinal Cancers Symposium abstract and poster describe a dose-escalation trial of GP-2250 (NCT03854110) in combination with gemcitabine in the 2nd-line treatment of metastatic pancreatic cancer patients who have progressed on or after FOLFIRINOX in the 1st-line treatment of the disease. The primary endpoints in the trial are the maximum tolerated dose ("MTD") and recommended Phase 3 dose.

"To date, we believe our GP-2250 has demonstrated strong effectiveness and safety in extensive preclinical studies, and its early clinical results have been encouraging for its initial indication for pancreatic cancer," said Greg Bosch, Chairman & Chief Executive Officer of Panavance. "We’re pleased with the progress of our ongoing Phase 1 trial which is currently at the 6th dose level with more than 20 patients enrolled thus far."

While Panavance’s initial area of focus is on pancreatic cancer, the company is conducting additional preclinical research in several other tumor types and expects to progress clinical development of GP-2250 for the treatment of other cancers.

Learn more about Panavance and GP-2250 at www.panavance.com.

References and links to websites have been provided for convenience, and the information contained on any such website is not a part of, or incorporated by reference into, this press release. Panavance is not responsible for the contents of third-party websites.

ITM Presents Study Design of COMPOSE Phase III Trial with ITM-11 (n.c.a. 177Lu-edotreotide) for Treatment of Neuroendocrine Tumors at ASCO-GI

On January 19, 2022 ITM Isotope Technologies Munich SE (ITM), a leading radiopharmaceutical biotech company, reported the presentation of the study design for its phase III trial, COMPOSE (NCT04919226), at the ASCO (Free ASCO Whitepaper) Gastrointestinal Cancers Symposium (ASCO-GI), held from January 20 – 22, 2022 (Press release, , 19 19, 2022, View Source [SID1234605661]). COMPOSE will evaluate the company’s lead radiopharmaceutical candidate, ITM-11 (n.c.a. 177Lu-edotreotide), compared to best standard of care in patients with well‐differentiated high grade 2 and grade 3 somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors (G2+G3 SSTR+ GEP-NETs). ITM-11 consists of the high-quality radioisotope, no-carrier-added lutetium-177 (n.c.a. 177Lu) chelated to the somatostatin analogue edotreotide. The aim of the study, in which patients are currently being randomized, is to evaluate the efficacy and safety of the Targeted Radionuclide Therapy in this high-need indication. COMPOSE is ITM’s second phase III trial with ITM-11 following and building upon COMPETE (NCT03049189), in patients with grade 1 and grade 2 GEP-NETs. Sponsor of the COMPOSE study is ITM’s subsidiary ITM Solucin GmbH.

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"We look forward to presenting the study design of COMPOSE to the medical and scientific community at ASCO (Free ASCO Whitepaper)-GI given the significant potential of ITM-11 as an innovative treatment modality"

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"We look forward to presenting the study design of COMPOSE to the medical and scientific community at ASCO (Free ASCO Whitepaper)-GI given the significant potential of ITM-11 as an innovative treatment modality," commented Philip E. Harris, MD PhD, Chief Medical Officer at ITM. "The favorable safety profile and efficacy signals observed to-date with our lead candidate give us reason to believe that ITM-11 can provide an important clinical benefit to patients diagnosed with this high-need indication and an advanced stage of this cancer."

COMPOSE (NCT04919226) is an international, prospective, randomized, controlled, open-label, multi-center phase III clinical trial to evaluate the efficacy, safety, and patient-reported outcomes of first or second-line treatment with ITM-11 compared to best standard of care in patients with well-differentiated high grade 2 and grade 3 (Ki-67 index 15-55), SSTR+ GEP-NETs. The study aims to randomize 202 patients 1:1 to ITM-11 or to best standard of care — either chemotherapy (CAPTEM or FOLFOX) or everolimus — according to the investigator’s choice. The primary endpoint of the study is progression-free survival (PFS), which will be assessed every 12 weeks from randomization onwards. Secondary outcome measures include overall survival (OS) up to two years after disease progression.

"With poor prognoses and limited treatment options for GEP-NETs, COMPOSE is an important step toward addressing a patient population with a high unmet medical need," commented Thorvardur Ragnar Halfdanarson, Principal Investigator of COMPOSE at the Mayo Clinic, Rochester, MN, USA. "Targeted Radionuclide Therapy continues to demonstrate promise for the treatment of hard-to-treat tumors. As such, I look forward to investigating its potential for patients with advanced GEP-NETs as we move ITM-11 through this Phase III trial."

Presentation information

Title: Pivotal phase III COMPOSE trial will compare 177Lu-edotreotide with best standard of care for well-differentiated aggressive grade 2 and grade 3 gastroenteropancreatic neuroendocrine tumor

Abstract No: TPS514

Poster No: P5

Session: Trials in Progress Poster Session B: Pancreas, Small Bowel, and Hepatobiliary Tract

Presenter: Thorvardur Ragnar Halfdanarson, Mayo Clinic, Rochester, MN, USA

– End –

About Targeted Radionuclide Therapy

Targeted Radionuclide Therapy is an emerging class of cancer therapeutics, which seeks to deliver radiation directly to the tumor while minimizing radiation exposure to normal tissue. Targeted radiopharmaceuticals are created by linking a therapeutic radioisotope to a targeting molecule (e.g., peptide, antibody, small molecule) that can precisely recognize tumor cells and bind to tumor-specific characteristics, like receptors on the tumor cell surface. As a result, the radioisotope accumulates at the tumor site and decays, releasing a small amount of ionizing radiation, thereby destroying tumor tissue. The highly precise localization enables targeted treatment with minimal impact to healthy surrounding tissue.

About ITM-11 (n.c.a. 177Lu-edotreotide)

ITM-11, ITM’s therapeutic radiopharmaceutical candidate being investigated in the phase III clinical studies COMPETE and COMPOSE, consists of two components: the medical radioisotope no-carrier-added lutetium-177 (n.c.a. 177Lu) and the targeting molecule edotreotide, a synthetic form of the peptide hormone somatostatin that targets neuroendocrine tumor-specific receptors. Edotreotide binds to these receptors and places the medical radioisotope n.c.a. lutetium-177 directly onto the diseased neuroendocrine cells so that it accumulates at the tumor site. N.c.a. lutetium-177 is internalized into the tumor cells and decays, releasing medical radiation (ionizing β-radiation) with a maximum radius of 1.7 mm and destroying tumor tissue. The highly precise localization can result in the healthy tissue surrounding the targeted tumor being minimally affected.

RenovoRx Announces Presentation at the 2022 SPECTRUM Conference Highlighting Its Innovative RenovoTAMP™ Therapy for Targeted Treatment of Cancer

On January 19, 2022 RenovoRx, Inc. ("RenovoRx" or the "Company") (Nasdaq: RNXT), a biopharmaceutical company and innovator in targeted cancer therapy, reported that Dr. Ripal Gandhi, M.D., FSIR, FSVM, a Principal Investigator in the Company’s Phase 3 TIGeR-PaC study, presented ‘Trans-arterial Treatment Option in Pancreas Cancer’ at the recent 2022 SPECTRUM Conference (Press release, Renovorx, 19 19, 2022, View Source [SID1234605660]). Dr. Gandhi is professor of Interventional Radiology at the Miami Cancer Institute and Miami Cardiac and Vascular Institute, Florida International University Herbert Wertheim College of Medicine. The 2022 SPECTRUM conference was held last weekend, January 14-16, 2022, at the Nobu Hotel in Miami Beach, Florida.

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Since 2018, Dr. Gandhi has played a pivotal role in the TIGeR-PaC clinical trial as the PI for the Miami Cancer Institute. The TIGeR-PaC study is evaluating the Company’s novel therapy platform, RenovoTAMP (RenovoRx Trans-Arterial Micro-Perfusion) as a potential treatment option for locally advanced pancreatic cancer (LAPC) that may extend patient survival, reduce the typical, often debilitating side-effects associated with systemic chemotherapy (delivered intra-venously), and ultimately improve quality of life for pancreatic cancer patients.

Dr. Gandhi’s presentation at the 2022 SPECTRUM Conference provides an overview of the RenovoTAMP platform and supportive published research. The presentation showcased RenovoRx’s RR1 Phase I/II and RR2 Observational Registry studies that suggests that when RenovoTAMP is used in combination with radiation therapy, arterial microvasculature may be reduced, thereby minimizing chemotherapy leakage during delivery, and increasing the chemotherapy directly reaching the tumor – resulting in targeted delivery and reduced systemic side effects. In addition, Dr. Gandhi also shared preliminary pharmacokinetic data (data describing the absorption, distribution, metabolism, and excretion of chemotherapy) from five patients in the TIGeR-PaC study, which demonstrates an approximate two-thirds reduction in systemic gemcitabine, when compared to systemic levels in historical control patients receiving traditional IV infusion of gemcitabine. This data suggests that by using RenovoTAMP for targeted delivery of chemotherapy, the systemic impacts of chemotherapy may be being reduced.

"We appreciate Dr. Gandhi, a recognized expert specializing in minimally invasive treatments for cancer, both in his role as a Principal Investigator for the TIGeR-PaC study supporting our patients and their families, and for his ongoing efforts to educate clinicians throughout the medical community on the potential for RenovoTAMP as an option for the treatment of their patients with LAPC, " stated Dr. Ramtin Agah, Chief Medical Officer and Co-Founder of RenovoRx. He continued, "Our foundational studies provided support for the potential for intra-arterial delivery via RenovoTAMP to improve patient survival and counter the tolerability issues inherent to chemotherapy, which improves quality of life for patients during this critical time. Our team continues to make progress enrolling our Phase 3 clinical trial and looks forward to reporting on the interim data read out."

View Dr. Gandhi’s presentation, titled "Trans-arterial Treatment Option in Pancreas Cancer," at View Source

About the 2022 SPECTRUM Conference

The SPECTRUM conference offers attendees a comprehensive review of a variety of oncological diseases, combined with the latest developments in medical, interventional and surgical therapeutic options across multiple disciplines. SPECTRUM is both didactic and interactive with panel discussions, instructive case presentations and hands-on workshops focused on hepatocellular carcinoma, lung cancer, metastatic colorectal cancer, cholangiocarcinoma and liver metastases, renal and prostate cancer, pancreatic cancer, neuroendocrine and musculoskeletal tumors.

Gamida Cell Provides Update on Omidubicel BLA Submission

On January 19, 2022 Gamida Cell Ltd. (Nasdaq: GMDA), an advanced cell therapy company committed to cures for cancer and other serious diseases, reported that following receipt of positive Type B meeting correspondence from the U.S. Food and Drug Administration (FDA) yesterday, the company plans to initiate a rolling Biologics License Application (BLA) submission for omidubicel, a potentially life-saving treatment for patients with blood cancers in need of stem cell transplant (Press release, Gamida Cell, 19 19, 2022, View Source [SID1234605659]). As previously disclosed, in late 2021 the FDA requested a revised analysis of the manufacturing data generated at Gamida Cell’s wholly owned commercial manufacturing facility to demonstrate the analytical comparability to the Lonza clinical manufacturing site that produced omidubicel for the Phase 3 study. Gamida Cell and the FDA have now reached alignment that analytical comparability has been established between the commercial manufacturing facility and the product that was manufactured for the Phase 3 study. Based on this demonstration of comparability, along with the positive clinical results of the Phase 3 study, the FDA has agreed that the initiation of a rolling BLA submission is appropriate. Additional clinical data will not be required to initiate the BLA submission.

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"We are very pleased that our productive interactions with the FDA have resulted in alignment on the omidubicel manufacturing comparability analysis and agreement to initiate a rolling submission of our BLA application," said Julian Adams, Ph.D., Chief Executive Officer of Gamida Cell. "Omidubicel is the first bone marrow transplant product to receive Breakthrough Therapy Designation from the FDA and has the potential to be the first FDA-approved advanced cell therapy for allogeneic bone marrow transplant. Initiating the BLA submission will move us one step closer toward bringing potentially curative therapies to patients. We plan to complete the full BLA submission in the first half of this year, which will be an important achievement for Gamida Cell and the bone marrow transplant community."

About Omidubicel

Omidubicel is an advanced cell therapy under development as a potential life-saving allogeneic hematopoietic stem cell (bone marrow) transplant solution for patients with blood cancers. Omidubicel is the first bone marrow transplant graft to receive Breakthrough Therapy Designation from the U.S. FDA and has also received Orphan Drug Designation in the U.S. and EU. For more information about omidubicel, please visit View Source

Omidubicel is an investigational therapy, and its safety and efficacy have not been established by the FDA or any other health authority.