Equillium Reports First Quarter 2021 Financial Results and Provides Clinical Development Update

On May 13, 2021 Equillium, Inc. (Nasdaq: EQ), a clinical-stage biotechnology company developing itolizumab to treat severe autoimmune and inflammatory disorders, reported financial results for the first quarter 2021, and provided an update on its clinical development programs (Press release, Equillium, MAY 13, 2021, View Source [SID1234579928]).

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"During the quarter, we announced the first of multiple data catalysts across three indications expected in 2021 for itolizumab, highlighting its potential broad therapeutic utility," said Bruce Steel, chief executive officer at Equillium. "Data from the Type A group of patients in the Phase 1b EQUALISE study, our first from subcutaneous delivery, showed favorable safety and tolerability results in systemic lupus erythematosus patients. It also demonstrated a dose-dependent reduction in the pharmacodynamic marker of CD6 expression on effector T cells, and that these results were consistent with the promising data generated from intravenous dosing of itolizumab in the EQUATE study in acute graft-versus-host disease (aGVHD). We now look ahead to the EQUATE study where we expect to announce topline data before the end of this quarter, followed by regulatory feedback on our proposed pivotal study in first-line treatment of aGVHD in mid-2021. In the second half of the year we expect to announce data from the Type B group of patients with lupus nephritis in the EQUALISE study along with data from the EQUIP study in uncontrolled asthma."

2021 Year-to-Date Corporate & Clinical Highlights:

Announced favorable data from the Type A group of patients with systemic lupus erythematosus in the EQUALISE study, where itolizumab:
Was found to be safe and well tolerated
Demonstrated a dose-dependent reduction of cell surface CD6 expression on effector T cells, a leading indicator of drug activity, consistent with its mechanism of action
Demonstrated changes in pharmacodynamic markers observed with subcutaneous dosing were consistent with intravenous dosing of itolizumab
Presented positive interim data from the EQUATE study in patients with acute graft-versus-host disease at the following conferences:
2021 Transplantation and Cellular Therapy Meetings Digital Experience
European Society for Blood and Marrow Transplantation
Completed a registered direct offering with Decheng Capital on February 5, 2021, which raised $29.9 million in net proceeds, strengthening Equillium’s balance sheet and extending its expected cash runway into the second half of 2023
Strengthened the company’s leadership, including the following additions since the beginning of this year:
Dolca Thomas, M.D., appointed as executive vice president of research and development and chief medical officer
Y. Katherine Xu, Ph.D., partner at Decheng Capital, appointed to Equillium’s board of directors
Upcoming Catalysts:

EQUATE Phase 1b study: topline data in first-line aGVHD, 1H 2021
Regulatory feedback on proposed pivotal study in first-line aGVHD, mid-2021
Initiate pivotal study in first-line aGVHD, 2H 2021*
EQUALISE Phase 1b study: interim data from Type B patients (lupus nephritis), 2H 2021
EQUIP Phase 1b study: topline data in uncontrolled asthma, 2H 2021
*Proposed protocol & timeline for site initiation contingent on regulatory review

First Quarter 2021 Financial Results

Research and development (R&D) expenses for the first quarter of 2021 were $5.9 million, compared with $4.7 million for the same period in 2020. The increase in the first quarter of 2021 compared to the same period in 2020 was driven by an increase in clinical development expenses, primarily related to the EQUATE and EQUALISE studies as well as purchases of drug product from Equillium’s collaboration partner, Biocon, for Equillium’s ongoing clinical trials, greater headcount expenses, and greater research and translational science expenses. Those increases were partially offset by a reduction in overhead costs, primarily travel, and lower consulting expenses.

General and administrative (G&A) expenses for the first quarter of 2021 were $2.8 million, compared with $2.7 million for the same period in 2020. The increase in the first quarter of 2021 compared to the same period in 2020 was driven by greater headcount expenses, partially offset by lower consulting expenses, legal fees, and travel expenses.

Net loss for the first quarter of 2021 was $9.0 million, or $(0.33) per basic and diluted share, compared with a net loss of $7.8 million, or $(0.45) per basic and diluted share for the same period in 2020. The increase in net loss was largely attributable to increased research and development expenses.

Cash used in operations for the first quarter of 2021 was $7.9 million compared to $8.3 million in the fourth quarter of 2020.

Cash, cash equivalents and short-term investments totaled $104.1 million as of March 31, 2021, compared to $82.2 million as of December 31, 2020. The increase was due to the registered direct offering with Decheng Capital in February 2021, which raised $29.9 million in net proceeds. Equillium believes that its cash and investments will be sufficient to fund its currently planned operations into the second half of 2023.

About Itolizumab
Itolizumab is a clinical-stage, first-in-class anti-CD6 monoclonal antibody that selectively targets the CD6-ALCAM pathway. This pathway plays a central role in modulating the activity and trafficking of T cells that drive a number of immuno-inflammatory diseases. Equillium acquired rights to itolizumab through an exclusive partnership with Biocon Limited.

CymaBay Welcomes Dennis D. Kim, MD, MBA as Chief Medical Officer

On May 13, 2021 CymaBay Therapeutics, Inc. (NASDAQ: CBAY), a clinical-stage biopharmaceutical company focused on developing therapies for liver and other chronic diseases with high unmet need, reported that medical and clinical leader Dennis D. Kim, MD, MBA, is joining the company as Chief Medical Officer (Press release, CymaBay Therapeutics, MAY 13, 2021, View Source [SID1234579944]).

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"Improving patient lives is at the core of CymaBay’s mission, and Dr. Kim’s medical, clinical and strategic leadership – including his understanding of the rare disease community, passion for patient care, and a successful track record supporting fundraising, investor relations and industry partnership efforts – will help us do just that," said Sujal Shah, CymaBay President and Chief Executive officer. "I’m thrilled to welcome Dr. Kim to our team and look forward to his leadership in advancing our current phase 3 program for seladelpar in PBC, as well as our pipeline of treatment options for liver diseases with high unmet need."

Dr. Kim has over 20 years of drug development experience most recently serving as Chief Medical Officer of clinical-stage biotech company Afyx Therapeutics, where he led clinical, medical and regulatory development for Rivelin, a novel mucoadhesive patch to deliver treatment for diseases such as oral lichen planus. In this role, he served as the company’s key representative in all external facing activities including business development, industry events and third-party initiatives.

Prior to his role at Afyx Therapeutics, Dr. Kim served as Chief Medical Officer of Emerald Biosciences (now Skye Bioscience), where he focused on developing proprietary, synthetic cannabinoid-derived treatments for glaucoma and other diseases. Dr. Kim led preclinical and clinical research and development for THC-VHS for treatment of glaucoma and CBD-VHS for other eye diseases. Previously, he served as Chief Medical Officer of Zafgen, leading the company’s San Diego operations and clinical/medical affairs for development of its methionine aminopeptidase 2 inhibitor platform for metabolic diseases such as type 2 diabetes and rare genetic disorder Prader-Willi Syndrome. He has also counseled numerous pharmaceutical and biotech companies in advisory roles and as a Board member.

"CymaBay’s talented team is poised to bring seladelpar to patients in need, and I am honored to join the company as it continues its phase 3 trials," Dr. Kim said. "The opportunity to impact the quality of life for thousands of patients and their families is what drew me to CymaBay – and that includes the exciting and promising pipeline of potential therapies for patients with liver disease and advancing more options for people in need."

Earlier in his career, Dr. Kim held senior leadership roles at Orexigen Therapeutics, where he served on the company’s Joint Commercialization Committee in partnership with Takeda Pharmaceuticals for U.S. commercialization of weight-loss treatment Contrave; EnteroMedics, where he was a key member of the executive team leading the company’s initial public offering; and Amylin Pharmaceuticals, where he managed corporate and business strategic planning across all developmental drug candidates for treatment of diabetes and obesity, and oversaw corporate alliance partnerships. He has also served as an Assistant Professor and Chief Endocrine Fellow at the University of California, San Diego School of Medicine.

Dr. Kim received his medical degree from The Chicago Medical School and completed his internal medicine residency at Rush University Medical College. He also holds a Master’s in Business Administration with emphasis in biotechnology structure and strategy from the University of California, San Diego Rady School of Business. He is a member of multiple professional societies, including the American College of Physicians, American Diabetes Association, American Association of Clinical Endocrinologists, and the Endocrine Society, and has authored more than 100 manuscripts, review articles and abstracts. Dr. Kim also serves on the Board of Directors for Inversago Pharma.

Seattle Cancer Care Alliance is an Authorized Treatment Center for Ide-cel CAR T-Cell Therapy

On May 13, 2021 Seattle Cancer Care Alliance (SCCA), the only National Comprehensive Cancer Network designated cancer center in Washington State, reported that it is an authorized treatment center for the new B-cell maturation antigen (BCMA) targeted chimeric antigen receptor (CAR) T-cell therapy, idecabtagene vicleucel, also known as ide-ce (Press release, Seattle Cancer Care Alliance, MAY 13, 2021, View Source [SID1234579962]).

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Ide-cel was approved by the U.S. Food and Drug Administration (FDA) on March 26, 2021, and is indicated for the treatment of adult patients with relapsed refractory multiple myeloma after four or more prior lines of therapy including a proteasome inhibitor, an immunomodulatory therapy and an anti-CD38 antibody. It is the first cell-based gene therapy approved by the FDA for the treatment of multiple myeloma and is being marketed under the brand name Abecma.

"We are pleased to offer this new advanced therapy to patients who are suffering from relapsed or refractory multiple myeloma," said Nancy Davidson, MD, president and executive director of Seattle Cancer Care Alliance. "We are committed to delivering personalized care to our patients and improving patient outcomes and excited to be among the first cancer centers in the nation to offer this treatment to adult patients with multiple myeloma."

Multiple myeloma is a cancer of plasma cells in which abnormal plasma cells build up in bone marrow and limit the body’s ability to make enough healthy blood cells, thus resulting in low blood counts. Multiple myeloma is also associated with bone and kidney damage as well as a weakened immune system. There are over 140,000 people in the United States living with this cancer and according the American Cancer Society approximately 34,920 new cases will be diagnosed in 2021, and 12,410 deaths among those with multiple myeloma will occur.

Ide-cel is a one-time therapy that is created from a patient’s own white blood cells, which have been modified to recognize and attack myeloma cells. As an anti-BCMA CAR T-cell therapy, ide-cel recognizes and binds to BCMA, a protein that is nearly universally expressed on cancer cells in multiple myeloma, leading to the death of BCMA-expressing cells.

In the clinical study that supported its approval, ide-cel was shown to be safe and effective. Approximately 72% of patients partially or completely responded to the treatment with 28% of patients showing complete response. An estimated 65% of this group remained in complete response to ide-cel for at least 12 months.

"The FDA approval of this novel therapy is a significant milestone in the advancement of new, innovative therapies for multiple myeloma," said David Maloney, MD, PhD, medical director for cellular immunotherapy at the Bezos Family Immunotherapy Clinic at Seattle Cancer Care Alliance. "We are excited about the continued expansion of CAR T-cell treatment options available to our patients, and the potential ide-cel offers to extend the lives of those who have multiple myeloma."

"Our clinical trials at the SCCA have provided us with extensive experience using BCMA CAR T-cells for multiple myeloma. The new FDA approval allows our to leverage this knowledge and safely bring a promising therapy to a wider population of adult patients with multiple myeloma," said Damian Green, MD, Seattle Cancer Care Alliance and Associate Professor, and who leads translational myeloma research programs at Seattle Cancer Care Alliance and the Fred Hutchinson Cancer Research Center.

SCCA is home to several of the world’s leading immunotherapy experts whose research has contributed to the foundation of many immunotherapies currently used to treat cancer. SCCA’s Bezos Family Immunotherapy Clinic, which opened in 2016, is a state-of-the-art center dedicated to offering the newest cellular immunotherapy clinical trials and FDA approved treatments.

Medtronic to Announce Financial Results for its Fourth Quarter and Full Fiscal Year 2021

On May 13, 2021 Medtronic plc (NYSE:MDT) reported that it will report financial results for its fourth quarter and full fiscal year 2021 on Thursday, May 27, 2021. A news release will be issued at approximately 5:45 a.m. Central Daylight Time (CDT) and will be available at View Source The news release will include summary financial information for the company’s fourth quarter and fiscal year 2021, which ended on Friday, April 30, 2021.

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Medtronic will host a video webcast at 7:00 a.m. CDT to discuss financial results for its fourth quarter and full fiscal year 2021. The webcast can be accessed at View Source on May 27, 2021.

Within 24 hours of the broadcast, a replay and transcript of the prepared remarks will be available by clicking on the Investor Events link at View Source.

Looking ahead, Medtronic plans to report its fiscal year 2022 first, second, third, and fourth quarter results on Tuesday, August 24, 2021, Tuesday, November 23, 2021, Tuesday, February 22, 2022, and Thursday, May 26, 2022, respectively. For these events, confirmation and additional details will be provided closer to the specific event.

Financial Results of Q1 FY2021

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