Aprea Therapeutics Highlights Positive Emerging Clinical Activity for WEE1 Inhibitor, APR-1051, with a Confirmed Partial Response in the Ongoing Phase 1 ACESOT-1051 Trial

On March 30, 2026 Aprea Therapeutics, Inc. (Nasdaq: APRE) ("Aprea", or the "Company"), a clinical-stage precision medicine oncology company focused on the discovery and development of targeted therapies for patients with biomarker-defined cancers, reported the confirmation of a partial response (PR) in its ongoing ACESOT-1051 trial evaluating APR-1051, a potent and selective WEE1 kinase inhibitor.

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The confirmed PR was observed in a patient with PPP2R1A-mutated endometrial cancer who is currently being treated at the 220 mg once daily dose level. Aprea announced on February 18, 2026 that, at their first imaging assessment, this patient achieved a 50% reduction in target lesion size (meeting RECIST criteria for partial response) as well as a reduction in CA-125 levels. This response was subsequently confirmed at the second image assessment, with an additional 9.5% reduction in target lesion size, and a reduction in CA-125 to 40.2U/ml (from 362 U/mL at baseline).

ACESOT-1051 is a biomarker focused Phase 1 trial designed to evaluate the safety, tolerability, pharmacokinetics, and preliminary anti-tumor activity of APR-1051 in patients with advanced solid tumors harboring cancer-associated genetic alterations. A total of 24 patients have been treated to date, at doses ranging from 10 mg to 220 mg once daily. Two patients have achieved partial responses, both with endometrial cancers harboring PPP2R1A mutations. One of these responses has been confirmed, as described above. Both patients remain on treatment.

Five other patients in ACESOT-1051 have achieved a best overall response of stable disease, including patients with HPV+ head and neck squamous cell carcinoma (HNSCC), colorectal and endometrial cancers with relevant genomic alternations. APR-1051 has been generally safe and well tolerated with the most common adverse events reported as Grade 1 or 2, primarily consisting of nausea and fatigue.

"The data emerging from the ACESOT-1051 trial continue to support the clinical potential of APR-1051, with confirmation of a partial response in the 220 mg cohort indicating evidence of sustained anti-tumor activity," said Eugene Kennedy, MD, Chief Medical Advisor at Aprea. "APR-1051 appears to be generally well-tolerated with an encouraging therapeutic window and overall, these findings strengthen our confidence in the ability of this candidate to successfully target WEE1 in genetically defined cancers, where patients face significant unmet need."

Dose escalation is ongoing, with plans to advance to Dose Level 9 (300 mg once daily) in the second quarter of 2026. In parallel, the company plans to enroll additional patients as specified in the protocol based on the understanding that their tumor types or specific mutations gives them an increased probability of responding to this class of potential therapeutics. This includes patients with uterine serous carcinoma (a subset of endometrial), colorectal and HPV+ tumors. For more information on ACESOT-1051, refer to ClinicalTrials.gov NCT06260514.

(Press release, Aprea, MAR 30, 2026, View Source [SID1234664017])

Anixa Biosciences Announces Presentation of its Ovarian Cancer CAR-T Therapy Clinical Trial at the Society of Gynecologic Oncology Annual Meeting on Women’s Cancer

On March 30, 2026 Anixa Biosciences, Inc. ("Anixa" or the "Company") (NASDAQ: ANIX), a biotechnology company focused on the treatment and prevention of cancer, reported that Dr. Robert Wenham, Chair of the Gynecologic Oncology Department at Moffitt Cancer Center and principal investigator for the Company’s ongoing ovarian cancer CAR-T therapy Phase 1 trial, will be presenting at the Society of Gynecologic Oncology (SGO) Annual Meeting on Women’s Cancer, being held April 10 – 13, 2026, in San Juan, Puerto Rico.

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Dr. Wenham’s presentation, titled "Phase 1 clinical trial of autologous T cells genetically engineered with a chimeric receptor to target the follicle-stimulating hormone receptor (FSHR) in recurrent ovarian cancer," will discuss the clinical trial design and objectives, as well as the current status of Anixa’s ongoing Phase 1 clinical trial of lira-cel.

The SGO Annual Meeting on Women’s Cancer stands as the foremost educational and scientific gathering for professionals dedicated to the treatment and care of individuals with gynecologic cancer, bringing together global experts in gynecologic oncology to share the latest scientific advancements, participate in educational programs, and network with peers.

About Lira-cel, Anixa’s CAR-T Therapy for Recurrent Ovarian Cancer
Liraltagene autoleucel, or lira-cel, uniquely targets the follicle-stimulating hormone receptor (FSHR), which is selectively expressed on ovarian cells, tumor vasculature, and certain cancer cells, but not in healthy tissue. The ongoing Phase 1 trial (ClinicalTrials.gov NCT05316129) is enrolling adult women with recurrent ovarian cancer who have progressed after at least two prior therapies.

(Press release, Anixa Biosciences, MAR 30, 2026, View Source [SID1234664016])

Insilico Medicine Announces Global R&D Collaboration with Lilly

On March 29, 2026 Insilico Medicine ("Insilico", HKEX: 3696), a clinical-stage biotechnology company powered by generative artificial intelligence (AI) and automation, reported a drug discovery collaboration with Eli Lilly and Company ("Lilly") that uses Insilico’s AI engine to accelerate the discovery and development of novel therapeutics across multiple therapeutic areas.

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The agreement grants Lilly an exclusive worldwide license for the development, manufacturing, and commercialization of potentially best-in-class, novel oral therapeutics in preclinical development for certain indications. In addition, Insilico and Lilly will collaborate on multiple R&D programs focused on targets selected by Lilly, by combining Insilico’s state-of-the-art Pharma.AI platforms with Lilly’s development capabilities and deep disease-area expertise.

"From its inception, Insilico Medicine has been developing deep learning for end-to-end drug discovery. By deploying frontier AI technologies that scale from biomarkers to life models, world models of human and animal life, we can identify multi-purpose targets driving multiple diseases at the same time," said Alex Zhavoronkov, PhD, founder and CEO of Insilico Medicine. "Working with Lilly, we aim to deliver transformative therapies that treat diseases with high unmet need. This collaboration is a testament to the power of AI in tackling the most complex challenges in human health."

Under the terms of the agreement, Insilico is eligible to receive an $115 million upfront payment, followed by development, regulatory, and commercial milestones that could bring the total deal value to approximately $2.75 billion, plus tiered royalties on future sales.

"Insilico’s AI-enabled discovery capabilities represent a powerful complement to Lilly’s deep expertise in clinical development across multiple therapeutic areas," said Andrew Adams, Group Vice President of Molecule Discovery at Lilly. "This collaboration allows us to explore novel mechanisms and accelerate the identification of promising therapeutic candidates across multiple disease areas."

(Press release, Insilico Medicine, MAR 29, 2026, View Source [SID1234664001])

ENHERTU® Followed by THP Approved in China as the First and Only HER2 Directed ADC for the Neoadjuvant Treatment of HER2 Positive Breast Cancer

On March 27, 2026 Daiichi Sankyo reported ENHERTU (trastuzumab deruxtecan) followed by paclitaxel, trastuzumab and pertuzumab (THP) has been approved in China for the neoadjuvant treatment (before surgery) of adult patients with HER2 positive (immunohistochemistry [IHC] 3+ or in-situ hybridization [ISH]+) stage 2 (high risk) or stage 3 breast cancer. This indication was granted conditional approval based on the DESTINYBreast11 phase 3 trial, which showed an improvement in pathologic complete response (pCR) rate. Full approval will depend on whether ongoing adjuvant studies confirm long-term clinical benefit in patients with early or locally advanced breast cancer.

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ENHERTU is a specifically engineered HER2 directed DXd antibody drug conjugate (ADC) discovered by Daiichi Sankyo (TSE: 4568) and being jointly developed and commercialized by Daiichi Sankyo and AstraZeneca (LSE/STO/NYSE: AZN).

Breast cancer is the second most common cancer in women in China, with approximately 357,000 cases of breast cancer diagnosed and nearly 75,000 deaths in 2022. 1 Approximately one in five cases of breast cancer is considered HER2 positive, a breast cancer subtype which is often associated with aggressive disease and poor prognosis. 2,3 For patients with HER2 positive early breast cancer, reaching a pCR with neoadjuvant treatment is the earliest indicator of improved long-term survival.4 However, approximately half of patients who receive neoadjuvant treatment do not reach pCR, putting them at increased risk of disease recurrence.

The conditional approval of ENHERTU by China’s National Medical Products Administration (NMPA) is based on results from the DESTINY-Breast11 phase 3 trial presented at the 2025 European Society for Medical Oncology (ESMO) (Free ESMO Whitepaper) Congress and simultaneously published in the Annals of Oncology.

In DESTINY-Breast11, ENHERTU followed by THP demonstrated a statistically significant and clinically meaningful improvement in pCR rate compared to dose-dense doxorubicin and cyclophosphamide followed by THP (ddAC-THP) in patients with high-risk HER2 positive early-stage breast cancer. The pCR rate with ENHERTU followed by THP was 67.29% compared to 56.25% with ddAC-THP, representing an improvement of 11.17% (95% confidence interval [CI]: 3.95-18.28; p=0.003). Similar improvement in pCR rate was observed across most prespecified subgroups, including hormone receptor positive and negative patients. At the time of the analysis, the secondary endpoint of event-free survival (EFS) was not mature (4.5% maturity at data cut-off). However, an early analysis showed a trend favoring ENHERTU followed by THP versus ddAC-THP (hazard ratio [HR]=0.56; 95% CI: 0.26-1.17). Efficacy results were consistent in the China subgroup.

"In patients with high-risk HER2 positive early-stage breast cancer, effective neoadjuvant treatment is critical to lower the risk of disease recurrence and maximize the chance of cure while potentially enabling less intensive surgery," said Professor Jiong Wu, Secretary of the Party Committee of Fudan University Shanghai Cancer Center and China leading primary investigator of the DESTINY-Breast11 trial. "Findings from DESTINY-Breast11 showed that approximately 67% of patients had a pathologic complete response with ENHERTU followed by THP, suggesting a potential new standard of care in this setting."

"As the first approval of ENHERTU globally for the neoadjuvant treatment of HER2 positive early-stage breast cancer and the first HER2 directed antibody drug conjugate approved in China in this setting, ENHERTU followed by THP offers patients in China a new treatment option with the opportunity to reach a pathologic complete response and the potential for improved long-term outcomes," said Michio Hayashi, China President, Daiichi Sankyo. "This third approval of ENHERTU in the last three months and seventh approval in three years reinforces the rapid progress we are making in bringing ENHERTU to more patients in China, where there is a high incidence of breast cancer and a continued need for new treatment approaches."

"ENHERTU followed by THP is the first treatment regimen in more than a decade to demonstrate a clinically meaningful improvement in pathologic complete response and safety in the neoadjuvant setting for patients with HER2 positive early-stage breast cancer, underscoring the significance of this new approval," said Dave Fredrickson, Executive Vice President, Oncology Hematology Business Unit, AstraZeneca. "ENHERTU is already an important option in the metastatic setting, and this decision will bring it into earlystage disease where cure is possible."

The safety profile of ENHERTU followed by THP in DESTINY-Breast11 was consistent with the known profiles of each individual therapy with no new safety concerns identified. The most common grade 3 or 4 adverse reactions in patients that received at least one dose of ENHERTU 5.4 mg/kg followed by THP in DESTINY-Breast11 (N=320) were neutropenia (13.8%), diarrhea (5.9%), increased transaminases (5.0%), leukopenia (4.4%), nausea (1.9%), peripheral neuropathy (1.9%) and anemia (1.6%). Grade 5 adverse reactions occurred in 0.3% of patients, including interstitial lung disease (ILD; 0.3%). The most frequent adverse reactions associated with permanent discontinuation were peripheral neuropathy (2.2%), ILD (1.9%) and increased transaminases (1.3%).

An application for ENHERTU followed by a taxane, trastuzumab and pertuzumab (THP) also is under review in the U.S. for the neoadjuvant treatment of patients with HER2 positive early-stage breast cancer based on the results from the DESTINY-Breast11 trial.

About DESTINY-Breast11
DESTINY-Breast11 is a global, multicenter, randomized, open-label, phase 3 trial evaluating the efficacy and safety of neoadjuvant ENHERTU (5.4 mg/kg) monotherapy or ENHERTU followed by THP compared to ddAC-THP in patients with high-risk HER2 positive early-stage breast cancer.

Patients were randomized 1:1:1 to receive either eight cycles of ENHERTU monotherapy; four cycles of ENHERTU followed by four cycles of THP; or four cycles of ddAC followed by four cycles of THP.

The primary endpoint of DESTINY-Breast11 is rate of pCR (absence of invasive disease in the breast and lymph nodes). Secondary endpoints include EFS, invasive disease-free survival, overall survival and safety.

DESTINY-Breast11 enrolled 927 patients across multiple sites in Asia, Europe, North America and South America. For more information about the trial, visit ClinicalTrials.gov.

About Neoadjuvant HER2 Positive Early Breast Cancer
Breast cancer is the second most common cancer and one of the leading causes of cancer-related deaths worldwide. 10 More than two million breast cancer cases were diagnosed in 2022, with more than 665,000 deaths globally.10 In China, breast cancer is the second most common cancer in women.1 Approximately 357,000 cases of breast cancer were diagnosed in China in 2022, with nearly 75,000 deaths.1

HER2 is a tyrosine kinase receptor growth-promoting protein expressed on the surface of many types of tumors including breast cancer.3 HER2 protein overexpression may occur as a result of HER2 gene amplification and is often associated with aggressive disease and poor prognosis in breast cancer. 3 Approximately one in five cases of breast cancer is considered HER2 positive.2

Approximately one in three patients with HER2 positive early-stage breast cancer is considered high-risk, meaning they are more likely to experience disease recurrence and have a poor prognosis.11 For patients with HER2 positive early breast cancer, reaching pCR with neoadjuvant treatment is the earliest indicator of improved long-term survival.4 However, approximately half of patients who receive neoadjuvant treatment do not reach pCR, putting them at increased risk of disease recurrence.

The current standard of care in the HER2 positive neoadjuvant setting in China consists of a combination regimen of carboplatin, trastuzumab, pertuzumab and a taxane.

(Press release, Daiichi Sankyo, MAR 27, 2026, View Source(5.4%20mg/kg)%20followed%20by%20THP%20is,HER2%20positive%20(IHC%203+%20or%20ISH+)%20stage [SID1234665018])

Agni Bio Selected to Present AGB101 (Vβ17 x DLL3) Poster at AACR Annual Meeting 2026

On March 27, 2026 Agni Bio, Inc., a biotechnology company developing next-generation immunotherapies, reported that it has been selected to present a poster highlighting its AGB101 (Vβ17 x DLL3) program at the AACR (Free AACR Whitepaper) Annual Meeting 2026 in the Late Breaking Poster Session, taking place April 17–22, 2026 in San Diego and hosted by the American Association for Cancer Research (AACR) (Free AACR Whitepaper).

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The poster will feature preclinical data for AGB101, a first-in-class Vβ17 x DLL3 bispecific antibody designed to selectively redirect a defined subset of cytotoxic memory T cells to tumors. Agni Bio plans to initiate a Phase 1 clinical trial of AGB101 in the second half of 2026.

Key Highlights from the Poster Presentation:

Novel mechanism of action: AGB101 selectively engages Vβ17 T cell receptor (TCR)–expressing T cells, a memory T cell subset with enhanced cytotoxicity, persistence, and resistance to exhaustion.
Targeted tumor approach: The molecule targets DLL3, a solid tumor lineage antigen highly expressed in small cell lung cancer (SCLC) and other neuroendocrine tumors.
Selective immune activation: Unlike CD3-directed bispecific antibodies which non-selectively redirects the majority of T cells, AGB101 selectively redirects and expands Vβ17 cells to drive DLL3-dependent cytotoxicity.
Reduced cytokine release profile: Preclinical studies with AGB101 demonstrate lower levels of release of pro-inflammatory cytokines (including TNF-α, IL-4, and IL-1β) while maintaining cytotoxic effector function (Granzyme B), suggesting the potential for an improved safety profile relative to CD3-based approaches.
Robust anti-tumor activity: AGB101 achieved potent and durable cytotoxicity in vitro and demonstrated complete tumor regressions in multiple DLL3-positive in vivo models.
Durable and memory-driven responses: Data show selective expansion (up to 10–15-fold) of Vβ17 T cells with a strong CD8+ bias and enhanced anti-tumor activity upon tumor rechallenge.
"AGB101 represents a fundamentally new approach to T cell redirection by selectively harnessing a highly functional subset of memory T cells," said Matt Lorenzi, PhD, Chief Scientific Officer and Board Member of Agni Bio. "We believe this strategy has the potential to overcome key limitations of first-generation T cell engagers, including toxicity and limited durability, and we are excited to advance this program into the clinic later this year."

AGB101 is part of Agni Bio’s Vβ17 platform of TCR-directed bispecific antibodies designed to improve the precision and effectiveness of immune engagement in cancer and autoimmune therapies.

(Press release, Agni Bio, MAR 27, 2026, View Source [SID1234664176])