GT Biopharma to Host Conference Call to Discuss Second Quarter 2021 Results

On August 6, 2021 GT Biopharma, Inc. ("GT Biopharma" or the "Company") (NASDAQ: GTBP), a clinical stage immuno-oncology company focused on developing innovative therapeutics based on the Company’s proprietary natural killer (NK) cell engager (TriKE) protein biologic technology platform, reported that the management team will host a conference call to discuss second quarter 2021 financial results and general business updates on August 13, 2021 at 8:30 a.m. EST (Press release, GT Biopharma, AUG 6, 2021, https://ir.gtbiopharma.com/news/detail/230/gt-biopharma-to-host-conference-call-to-discuss-second-quarter-2021-results [SID1234586003]).

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To join the call:

U.S. callers should dial 1-877-870-4263 and international callers should dial 1-412-317-0790.
All participants should ask to be connected to the GT Biopharma conference call.
The call will be available by visiting the "Presentations" page in the "News & Media" section of GT Biopharma’s website at www.gtbiopharma.com/news-media/presentations. A replay of the call will be archived for 30 days following the presentation.

Spectrum Pharmaceuticals Receives Complete Response Letter from FDA for ROLONTIS® (eflapegrastim)

On August 6, 2021 Spectrum Pharmaceuticals (NasdaqGS: SPPI), a biopharmaceutical company focused on novel and targeted oncology therapies, reported receipt of a Complete Response Letter (CRL) from the U.S. Food and Drug Administration (FDA) regarding the company’s Biologics License Application (BLA) for ROLONTIS (eflapegrastim). The CRL cited deficiencies related to manufacturing and indicated that a reinspection will be necessary. The company is seeking further clarification from the FDA and plans to meet with the agency as soon as possible.

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"We are disappointed with this outcome and look forward to fully understanding the remediation timelines for the program," said Joe Turgeon, President and CEO of Spectrum Pharmaceuticals. "We continue to believe in ROLONTIS and plan to diligently complete the regulatory process to bring ROLONTIS to market."

About ROLONTIS

ROLONTIS is a novel, long-acting granulocyte colony-stimulating factor (G-CSF) seeking an indication for the treatment of neutropenia in patients receiving myelosuppressive anti-cancer drugs. The BLA for ROLONTIS is supported by data from two identically designed Phase 3 clinical trials, ADVANCE and RECOVER, which evaluated the safety and efficacy of ROLONTIS in 643 early-stage breast cancer patients for the treatment of neutropenia due to myelosuppressive chemotherapy. In both studies, ROLONTIS demonstrated the pre-specified hypothesis of non-inferiority (NI) in duration of severe neutropenia (DSN) and a similar safety profile to pegfilgrastim. ROLONTIS also demonstrated non-inferiority to pegfilgrastim in the DSN across all 4 cycles (all NI p<0.0001) in both trials.

Artificial Intelligence aids in discovery of new prognostic biomarkers for breast cancer

On August 6, 2021 Scientists at Case Western Reserve University reported that they have used Artificial Intelligence (AI) to identify new biomarkers for breast cancer that can predict whether the cancer will return after treatment—and which can be identified from routinely acquired tissue biopsy samples of early-stage breast cancer (Press release, Case Western Reserve University, AUG 6, 2021, View Source [SID1234586000]).

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The key to that initial determination is collagen, a common protein found throughout the body, including in breast tissue. Previous research had suggested that the collagen network, or arrangement of the fibers, relates strongly to breast cancer aggressiveness. But this work by Case Western Reserve researchers definitively demonstrated collagen’s critical role—using only standard tissue biopsy slides and AI.

The researchers, using machine-learning technology to analyze a dataset of digitized tissue samples from breast cancer patients, were able to prove that a well-ordered arrangement of collagen is a key prognostic biomarker for an aggressive tumor and a likely recurrence.

Conversely, they showed that a disordered or broken-down collagen infrastructure not only indicates a better outcome, but actually promotes one. They also found that the disordered collagen network prevents an otherwise aggressive tumor from migrating out of the breast tissue and helps prevent its return after various cancer treatments like chemotherapy.

Haojia Li
"It sounds counter-intuitive, but the collagen fibers play a role in tumor migration," said Anant Madabhushi, the Donnell Institute Professor of Biomedical Engineering at Case Western Reserve and head of the Center for Computational Imaging and Personalized Diagnostics (CCIPD). "One way to understand it is to say that if the collagen ‘highway’ is in terrible shape, it’s more difficult for the tumor to migrate, but if it’s smooth and organized, it makes it easier for the tumor to hitch a ride."

Doctoral student Haojia Li led the research, which was published in the journal npj Breast Cancer. Other authors included Pingfu Fu, professor of Population and Quantitative Health Sciences at the Case Western Reserve School of Medicine, and others from several institutions.

Simple tissue slides, complex computing

Li said the project was important because:

It validates findings from other published research that suggested highly organized collagen indicates a worse prognosis.
It was accomplished with digitized images of those simple tissue slides, suggesting this method could become part of a pathologist’s routine. Current methods for examining and investigating the collagen architecture require an expensive and less common electron microscope.
"Our method would make predicting outcomes much more available to more doctors and in hospitals which don’t have the resources to have an advanced imaging microscope," Li said. "That’s why this is so exciting—because it can give the physician the information he or she needs to guide how aggressively to treat the cancer."

The computational work was done in 2020, based on a dataset of routine tissue samples, known as H&E (hematoxylin and eosin) stain slides, taken from patients diagnosed with early stage Estrogen Receptor Positive (ER+) breast cancer.

Breast cancer is the second leading cause of cancer death among women in the United States, with approximately 80% of these cancers being ER+ and 64% being early stage, Li said.

Anant Madabhushi
Anant Madabhushi
Madabhushi said that because the models built by his team were validated on a completed clinical trial data set, it would "provide a higher level of evidence with regard to the validity of the Collagen signature" and that it would also function as a "natural segue into prospective clinical trial validation."

Madabhushi established the CCIPD at Case Western Reserve in 2012. The lab now includes over 70 researchers and is a global leader in the detection, diagnosis and characterization of various cancers and other diseases, including breast cancer, by meshing medical imaging, machine learning and AI.

Some of the lab’s most recent work, in collaboration with New York University and Yale University, has used AI to predict which lung cancer patients would benefit from adjuvant chemotherapy based on tissue-slide images. That advancement was named by Prevention Magazine as one of the top 10 medical breakthroughs of 2018.

Aprea Therapeutics Announces a Partial Clinical Hold on Myeloid Malignancy Programs

On August 6, 2021 Aprea Therapeutics, Inc. (Nasdaq: APRE), a biopharmaceutical company focused on developing and commercializing novel cancer therapeutics that reactivate mutant tumor suppressor protein, p53, reported that the U.S. Food and Drug Administration (FDA) has placed a partial clinical hold on its clinical trials of eprenetapopt in combination with azacitidine in its myeloid malignancy programs (Press release, Aprea, AUG 6, 2021, View Source [SID1234585999]). The partial clinical hold does not apply to the Company’s ongoing clinical trials in lymphoid malignancies and solid tumors, or the APR-548 clinical trial.

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There are approximately 20 patients currently receiving eprenetapopt in combination with azacitidine in the Company’s myeloid malignancy programs, which includes the MDS, AML and post-transplant maintenance trials, all of which have completed enrollment. Patients who are benefiting from treatment can continue to receive study treatment. As part of the clinical hold, no additional patients can be enrolled to these trials until the partial clinical hold is resolved. Aprea intends to work closely with the FDA to analyze the data, address the specific questions raised, and seek to resolve the partial clinical hold as soon as possible.

"Patient safety is our highest priority," said Christian S. Schade, Chairman and Chief Executive Officer of Aprea. "Based on the totality of the data we have for eprenetapopt, we believe that it continues to be a promising therapeutic option for cancer patients. We are working closely with the FDA to review the data specific to eprenetapopt with azacitidine in our myeloid malignancy trials and will provide an update when we have additional information."

The Company will host a webcast conference call to discuss this announcement on August 6, 2021 at 8:30 AM (ET). Connection details are provided below and are also available on the Events page of Aprea’s website.

Ascendis Pharma A/S Announces Upcoming Investor Presentations in August

On August 6, 2021 Ascendis Pharma A/S (Nasdaq: ASND), a biopharmaceutical company that utilizes its innovative TransCon technologies to create new product candidates that address unmet medical needs, reported that the company will participate in two upcoming investor conferences in August (Press release, Ascendis Pharma, AUG 6, 2021, View Source [SID1234585982]). Company executives will provide a business overview and update on the company’s pipeline programs.

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Details

Event 2021 Wedbush PacGrow Healthcare Conference
Location Virtual
Date Wednesday, August 11, 2021
Time 9:10 a.m. Eastern Time

Event Canaccord Genuity 41st Annual Growth Conference
Location Virtual
Date Thursday, August 12, 2021
Time 11:00 a.m. Eastern Time
A live webcast of the presentations will be available in the Investors and News section of the Ascendis Pharma website at www.ascendispharma.com. A webcast replay will also be available on this website shortly after conclusion of the events for 30 days.