KEY NARMAFOTINIB PATENT GRANTED IN US

On December 2, 2025 Amplia Therapeutics Limited (ASX:ATX; OTCQB:INNMF), ("Amplia" or the "Company"), reported that it has received formal notification from the US Patent and Trademark Office (USPTO) that a key patent titled A salt and crystal form of a FAK Inhibitor has been granted.The Certificate of Grant follows on from the notification of allowance of the patent from the USPTO received in September.

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This key patent protects the specific form of narmafotinib being developed clinically by the Company. The patent has already been granted in various important jurisdictions including Europe, Japan, India, Korea and Australia. Granting of this patent extends protection of narmafotinib out to a least 2040 in these jurisdictions. Protection in other regions is under review by the respective patent offices.

Amplia CEO Dr Chris Burns says: "With the granting of this patent in the US and other key pharmaceutical markets, we are strengthening narmafotinib’s patent portfolio to protect and maximise the Company’s intellectual property for the long term."

(Press release, Amplia Therapeutics, DEC 2, 2025, View Source [SID1234661058])

Aurigene Oncology Limited Announces Encouraging Initial Data From 1st Two Cohorts of Phase 1 Study of AUR112, an Oral Small Molecule inhibitor of MALT1, in Relapsed/Refractory Lymphoid Malignancies

On December 2, 2025 Aurigene Oncology Limited, a clinical-stage biopharmaceutical company developing novel therapies in oncology, reported initial clinical results from 1st two cohorts of its ongoing Phase 1 clinical trial evaluating AUR112 in patients with relapsed or refractory lymphoid malignancies. Early findings show that AUR112 is safe, well tolerated, demonstrating meaningful clinical activity, with objective responses observed across multiple lymphoma subtypes, including Mantle Cell Lymphoma (MCL) and Marginal Zone Lymphoma (MZL).

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"We are very encouraged by the early results of the first two cohorts from our Phase 1 study of AUR112," said Dr. Murali Ramachandra, CEO. "AUR112 has shown a promising initial clinical profile, achieving an overall response rate of 63.6% in the efficacy-evaluable population and 58.3% in the intent-to-treat group. These strong early data, combined with its distinct preclinical and safety characteristics, reinforce our belief that AUR112 has the potential to become a best-in-class MALT1 inhibitor."

Study Design and Key Findings

The company is currently conducting a Phase 1 dose-escalation study evaluating AUR112 monotherapy in patients with relapsed/refractory lymphoid malignancies. Primary objectives include characterizing safety and identifying dose-limiting toxicities and secondary objectives include pharmacokinetics, pharmacodynamics, objective response rate, duration of response, and disease control rate.

As of the November 21, 2025 cutoff, 13 patients were evaluable for safety and 11 patients were evaluable for efficacy across three dose cohorts (100 mg, 200 mg, and 400 mg).

Safety: AUR112 was generally well tolerated. While 84.6% of patients experienced Treatment Emergent Adverse Events (TEAEs), only 14 events in 7 patients were treatment-related. No Grade 3 or higher hyperbilirubinemia was observed, and bilirubin elevations resolved even with continued treatment. One dose-limiting toxicity (DLT) (Grade 3 neutropenia) and two DLT-equivalent events were reported.
Pharmacokinetics/Pharmacodynamics: Drug exposure at 200 mg appears to be in the efficacious range, however further results are awaited. Pharmacodynamic data demonstrated rapid and sustained IL-2 inhibition, with all evaluated patients showing IL-2 levels below the limit of quantification by Cycle 1 Day 15.
Efficacy: Among 11 efficacy-evaluable patients (all in 1st two cohorts), the overall response rate was 63.6%, including six partial responses and one complete response. Responses were observed in MCL, MZL, Hodgkin Lymphoma (HL), and Diffuse Large B-Cell Lymphoma (DLBCL).
Based on these encouraging results, the initiation of dose-expansion cohorts in select lymphoid malignancies, including Chronic Lymphocytic Leukemia (CLL), Waldenström’s Macroglobulinemia, MCL, and MZL are being planned.

About AUR112

AUR112 is an oral investigational MALT1 inhibitor designed to target a pivotal signaling node in the NF-κB pathway. Through highly potent and selective inhibition of MALT1, AUR112 aims to disrupt survival mechanisms that drive B-cell malignancies. In preclinical studies, AUR112 exhibited significant monotherapy activity and demonstrated a favorable safety profile.

(Press release, Aurigene Discovery Technologies, DEC 2, 2025, View Source [SID1234661041])

Jazz Pharmaceuticals to Present Pivotal Phase 3 Results of Ziihera® (zanidatamab-hrii) Combinations in First-Line HER2-Positive Locally Advanced or Metastatic Gastroesophageal Adenocarcinoma at the 2026 ASCO Gastrointestinal Cancers Symposium

On December 2, 2025 Jazz Pharmaceuticals plc (Nasdaq: JAZZ) reported two abstracts featuring key data for Ziihera (zanidatamab-hrii) have been accepted for presentation at the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Gastrointestinal Cancers Symposium (ASCO GI) from January 8-10, 2026, in San Francisco. The Phase 3 HERIZON-GEA-01 trial results in first-line HER2-positive (HER2+) locally advanced or metastatic gastroesophageal adenocarcinoma (GEA) were accepted as a late-breaking presentation. Additionally, a new post-hoc overall survival (OS) analysis from the HERIZON-BTC-01 Phase 2b trial in previously treated HER2+ biliary tract cancer (BTC) will be presented, providing further information for this approved indication.

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"We look forward to sharing the clinically meaningful results from the Phase 3 HERIZON-GEA-01 trial with the oncology community at ASCO (Free ASCO Whitepaper) GI," said Rob Iannone, M.D., M.S.C.E., executive vice president, global head of research and development, and chief medical officer of Jazz Pharmaceuticals. "Advanced HER2+ GEA, which includes cancers of the stomach, gastroesophageal junction and esophagus, remains an aggressive cancer with a poor prognosis and continues to be an area with limited progress for patients. This trial was designed to evaluate whether Ziihera plus chemotherapy, with or without tislelizumab, could improve on the current standard of care in first-line therapy. We believe these positive results support Ziihera as the HER2-targeted agent-of-choice and the Ziihera combinations to become the new standard of care for patients with HER2+ first-line metastatic GEA regardless of PD-L1 status. Alongside new analyses from the HERIZON-BTC-01 Phase 2b trial, these presentations highlight the continued impact of our broad zanidatamab clinical program and our commitment to advancing innovation across HER2-targeted cancers."

The Phase 3 HERIZON-GEA-01 trial, conducted jointly with BeOne Medicines, is evaluating Ziihera in combination with chemotherapy, with or without the PD-1 inhibitor Tevimbra (tislelizumab), as first-line treatment for HER2+ locally advanced or metastatic GEA. As previously announced, both Ziihera plus chemotherapy and Ziihera plus tislelizumab and chemotherapy demonstrated highly statistically significant and clinically meaningful improvements in progression-free survival (PFS) compared to the control arm, trastuzumab plus chemotherapy. Ziihera plus tislelizumab and chemotherapy also demonstrated clinically meaningful and statistically significant improvements in overall survival (OS), and Ziihera plus chemotherapy demonstrated a clinically meaningful effect with a strong trend toward statistical significance for OS compared to the control arm at the time of this first analysis.

Jazz Pharmaceuticals will host an investor webcast on Friday, January 9, at 6:30 a.m. PT/ 9:30 a.m. ET to review the Ziihera data presented at the meeting. The webcast will include commentary from the company’s senior management and Dr. Geoffrey Ku, Associate Attending physician on the Gastrointestinal Oncology Service in the Department of Medicine at Memorial Sloan Kettering Cancer Center. The webcast may be accessed from the Investors section of the Jazz Pharmaceuticals website at www.jazzpharmaceuticals.com. To ensure a timely connection, it is recommended that participants register at least 15 minutes prior to the scheduled webcast.

A replay of the webcast will be available via the Investors section of the Jazz Pharmaceuticals website.

Details for both presentations can be found online and below:

Presentation Title

Authors

Presentation Details

Zanidatamab (zani) +
chemotherapy
(chemo) ± tislelizumab
(tisle) for first-line (1L)
HER2-positive
(HER2+)
advanced/metastatic
gastroesophageal
adenocarcinoma
(mGEA): first results
from the phase 3
HERIZON-GEA-01
study

Elena Elimova, Sun Young Rha, Kohei
Shitara, Tianshu Liu, Josep Tabernero,
Keun-Wook Lee, Michael Schenker, Niall
Tebbutt, Jaffer Ajani, Norhidayu Bt
Salimin, Geoffrey Ku, Jong Gwang Kim,
Inmaculada Ales Diaz, Jingdong Zhang,
Filippo Pietrantonio, Li-Yuan Bai, Samuel
Le Sourd, Ye Chen, Jonathan Grim, Lin
Shen, on behalf of the HERIZON-GEA-01
study group

Type: Late-Breaking Abstract
Oral Presentation

Session: Oral Abstract Session
A: Cancers of the Esophagus
and Stomach

Date: Thursday, Jan. 8, 8:57-
9:07 a.m. PST

Abstract number: LBA285

Landmark analysis of
overall survival (OS)
by objective response
in patients (pts) with
previously treated,
advanced HER2-
positive biliary tract
cancer (BTC): post
hoc analysis of the
HERIZON-BTC-01
trial

James J Harding, Jia Fan, Do-Youn Oh,
Hye Jin Choi, Jin Won Kim, Heung-Moon
Chang, Lequn Bao, Hui-Chuan Sun,
Teresa Macarulla, Feng Xie, Jean-
Philippe Metges, Jie’er Ying, John
Bridgewater, Harpreet Singh Wasan,
Michel Pierre Ducreux, Zinan Bao, Phillip
M Garfin, Douglas S Fuller, Parveen
Jayia, Shubham Pant

Type: Poster Session

Session: Poster Session B:
Cancers of the Pancreas, Small
Bowel, and Hepatobiliary Tract

Date: Friday, Jan. 9, 11:30 a.m.-1:00
p.m. PST

Abstract number: 545

The majority of abstracts accepted to ASCO (Free ASCO Whitepaper) GI will be released at 2:00 p.m. PT/ 5:00 p.m. ET on January 5, 2026. Late-breaking abstracts will be released at 7:00 a.m. PT / 10:00 a.m. ET on their day of presentation at the Symposium and made publicly available online at that time.

About Gastroesophageal Adenocarcinoma
GEA, including cancers of the stomach, gastroesophageal junction, and esophagus, is the fifth most common cancer worldwide, and approximately 20% of patients have HER2+ disease.1,2,3 HER2+ GEA has high morbidity and mortality, and patients are urgently in need of new treatment options. The overall prognosis for patients with GEA remains poor, with a global five-year survival rate of less than 30% for gastric cancer and about 19% for GEA.4

About Biliary Tract Cancer
BTC, which includes gallbladder cancer and intrahepatic and extrahepatic cholangiocarcinoma, are rare and aggressive epithelial tumors often associated with poor prognosis.5,6 Although they account for less than 1% of all human cancers, cholangiocarcinoma is the second most common primary liver cancer after hepatocellular carcinoma and comprises approximately 10–15% of all primary liver cancers. Global mortality from BTC has risen in recent decades.7

Because early symptoms are often vague or nonspecific, most BTCs are diagnosed at an advanced stage,8 when curative surgery is not an option.6,9,10 While chemotherapy and, more recently, immunotherapy-based combinations are used in the first-line setting, disease progression is common. In the absence of molecular profiling, treatment options following first-line therapy are largely limited to chemotherapy.7,9,11

HER2 overexpression or amplification defines a distinct molecular subtype of BTC12 and is observed in approximately 26% of patients globally.13 HER2-positive BTC is associated with worse prognosis than HER2-negative disease.14 Across the U.S., Europe, and Japan, an estimated 12,000 people are diagnosed with HER2-positive BTC each year.15

About Ziihera (zanidatamab-hrii)
Ziihera (zanidatamab-hrii) is a bispecific HER2-directed antibody that binds to two extracellular sites on HER2. Binding of zanidatamab-hrii with HER2 results in internalization leading to a reduction in HER2 expression of the receptor on the tumor cell surface. Zanidatamab-hrii induces complement-dependent cytotoxicity (CDC), antibody-dependent cellular cytotoxicity (ADCC), and antibody-dependent cellular phagocytosis (ADCP). These mechanisms result in tumor growth inhibition and cell death in vitro and in vivo.16 In the United States, Ziihera is indicated for the treatment of adults with previously treated, unresectable or metastatic HER2-positive (IHC 3+) BTC, as detected by an FDA-approved test.16 The U.S. FDA granted accelerated approval for this indication based on overall response rate and duration of response. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).16

Zanidatamab is being developed in multiple clinical trials as a targeted treatment option for patients with solid tumors that express HER2. Zanidatamab is being developed by Jazz Pharmaceuticals and BeOne Medicines under license agreements from Zymeworks Inc., which first developed the molecule.

The FDA granted Breakthrough Therapy designation for zanidatamab’s development in patients with previously treated HER2 gene-amplified BTC, and two Fast Track designations for zanidatamab: one as a single agent for refractory BTC and one in combination with standard-of-care chemotherapy for first-line GEA. Additionally, zanidatamab has received Orphan Drug designations from the FDA for the treatment of BTC and GEA, as well as Orphan Drug designation from the European Medicines Agency for the treatment of BTC and gastric cancer.

Important Safety Information for ZIIHERA

WARNING: EMBRYO-FETAL TOXICITY
Exposure to ZIIHERA during pregnancy can cause embryo-fetal harm. Advise patients
of the risk and need for effective contraception.

WARNINGS AND PRECAUTIONS

Embryo-Fetal Toxicity
ZIIHERA can cause fetal harm when administered to a pregnant woman. In literature reports, use of a HER2-directed antibody during pregnancy resulted in cases of oligohydramnios and oligohydramnios sequence manifesting as pulmonary hypoplasia, skeletal abnormalities, and neonatal death.

Verify the pregnancy status of females of reproductive potential prior to the initiation of ZIIHERA. Advise pregnant women and females of reproductive potential that exposure to ZIIHERA during pregnancy or within 4 months prior to conception can result in fetal harm. Advise females of reproductive potential to use effective contraception during treatment with ZIIHERA and for 4 months following the last dose of ZIIHERA.

Left Ventricular Dysfunction
ZIIHERA can cause decreases in left ventricular ejection fraction (LVEF). LVEF declined by >10% and decreased to <50% in 4.3% of 233 patients. Left ventricular dysfunction (LVD) leading to permanent discontinuation of ZIIHERA was reported in 0.9% of patients. The median time to first occurrence of LVD was 5.6 months (range: 1.6 to 18.7). LVD resolved in 70% of patients.

Assess LVEF prior to initiation of ZIIHERA and at regular intervals during treatment. Withhold dose or permanently discontinue ZIIHERA based on severity of adverse reactions.

The safety of ZIIHERA has not been established in patients with a baseline ejection fraction that is below 50%.

Infusion-Related Reactions
ZIIHERA can cause infusion-related reactions (IRRs). An IRR was reported in 31% of 233 patients treated with ZIIHERA as a single agent in clinical studies, including Grade 3 (0.4%), and Grade 2 (25%). IRRs leading to permanent discontinuation of ZIIHERA were reported in 0.4% of patients. IRRs occurred on the first day of dosing in 28% of patients; 97% of IRRs resolved within one day.

Prior to each dose of ZIIHERA, administer premedications to prevent potential IRRs. Monitor patients for signs and symptoms of IRR during ZIIHERA administration and as clinically indicated after completion of infusion. Have medications and emergency equipment to treat IRRs available for immediate use.

If an IRR occurs, slow, or stop the infusion, and administer appropriate medical management. Monitor patients until complete resolution of signs and symptoms before resuming. Permanently discontinue ZIIHERA in patients with recurrent severe or life-threatening IRRs.

Diarrhea
ZIIHERA can cause severe diarrhea.

Diarrhea was reported in 48% of 233 patients treated in clinical studies, including Grade 3 (6%) and Grade 2 (17%). If diarrhea occurs, administer antidiarrheal treatment as clinically indicated. Perform diagnostic tests as clinically indicated to exclude other causes of diarrhea. Withhold or permanently discontinue ZIIHERA based on severity.

ADVERSE REACTIONS
Serious adverse reactions occurred in 53% of 80 patients with unresectable or metastatic HER2-positive BTC who received ZIIHERA. Serious adverse reactions in >2% of patients included biliary obstruction (15%), biliary tract infection (8%), sepsis (8%), pneumonia (5%), diarrhea (3.8%), gastric obstruction (3.8%), and fatigue (2.5%). A fatal adverse reaction of hepatic failure occurred in one patient who received ZIIHERA.

The most common adverse reactions in 80 patients with unresectable or metastatic HER2-positive BTC who received ZIIHERA (≥20%) were diarrhea (50%), infusion-related reaction (35%), abdominal pain (29%), and fatigue (24%).

USE IN SPECIFIC POPULATIONS

Pediatric Use
Safety and efficacy of ZIIHERA have not been established in pediatric patients.

Geriatric Use
Of the 80 patients who received ZIIHERA for unresectable or metastatic HER2-positive BTC, there were 39 (49%) patients 65 years of age and older. Thirty-seven (46%) were aged 65-74 years old and 2 (3%) were aged 75 years or older.

No overall differences in safety or efficacy were observed between these patients and younger adult patients.

The full U.S. Prescribing Information for ZIIHERA, including BOXED Warning, is available at: View Source

TEVIMBRA (tislelizumab) is a registered trademark of BeOne Medicines.

(Press release, Jazz Pharmaceuticals, DEC 2, 2025, View Source [SID1234661060])

Black Diamond Therapeutics to Host Webcast Presentation Highlighting Silevertinib Phase 2 Clinical Trial Results and Program Update

On December 2, 2025 Black Diamond Therapeutics, Inc. (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, reported it will host a webcast to present results from its Phase 2 clinical trial of silevertinib and provide a program update on Wednesday, December 3, 2025, at 8:00am ET.

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Webcast information

The webcast can be accessed under "Events and Presentations" on the Investors section of the Black Diamond website at www.blackdiamondtherapeutics.com. A replay of the webcast will be available following the completion of the event.

(Press release, Black Diamond Therapeutics, DEC 2, 2025, View Source [SID1234661042])

Lunit to Highlight New AI Evidence in Cancer Screening and Breast Density-Driven Risk Modeling at RSNA 2025

On December 2, 2025 Lunit, a leading provider of AI for cancer diagnostics and precision oncology, reported it will present 14 studies at the Radiological Society of North America (RSNA) 2025 Annual Meeting. Spanning screening mammography, digital breast tomosynthesis (DBT), breast density science, and risk modeling, this year’s program represents one of the company’s most extensive evidence portfolios to date. Lunit will exhibit at South Hall, Booth #4100, and host expert-led sessions in the Lunit Education Room #1252 throughout the meeting.

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Among the highlighted research, real-world results from Capio S:t Göran Hospital in Sweden evaluated more than 193,000 screening examinations before and after the introduction of Lunit INSIGHT MMG. When AI was paired with a single radiologist, the screening program achieved higher invasive cancer detection, greater positive predictive value, and fewer unnecessary recalls compared to human-only double reading—reinforcing findings from the ScreenTrustCAD interventional trial and demonstrating that AI-integrated single reading can maintain or improve accuracy while alleviating workforce pressure.

New evidence from Massachusetts General Hospital assessed AI performance on screening DBT using 1,000 retrospective examinations, showing that Lunit INSIGHT DBT correctly localized 84.4% of true-positive cancers, with particularly strong performance for mass-presenting and invasive ductal carcinoma cases. The study also detailed cancer subtypes less likely to be identified by AI, offering practical insight into the algorithm’s strengths and limitations as DBT adoption accelerates worldwide.

Further expanding the evidence base, two oral presentations from Elizabeth Wende Breast Care explored how volumetric breast density, as quantified by AI-powered algorithms, and family history influence risk stratification across leading models, and how density changes over time affect prediction consistency. In a cohort of 44,651 women, Tyrer-Cuzick classified substantially more women as high-risk than BOADICEA, driven by heavier weighting of density and family history inputs. A complementary longitudinal analysis of 335,000+ images demonstrated that incorporating volumetric breast density over time improved calibration and discrimination, while static or categorical density inputs consistently underestimated cancer incidence. Together, these findings strengthen the role of density-informed and longitudinal risk modeling in supporting risk-adapted screening strategies.

Lunit will also host a series of expert-led sessions in its Education Room #1252, offering deeper clinical and scientific perspectives on key themes presented at RSNA. Highlights include:

Image-Based Risk (Nov 30, 1:30–2:00 PM CST)

A cross-disciplinary discussion featuring Drs. Graham Colditz, Joy Jiang, and Hari Trivedi, exploring how image-based risk complements traditional models and what this means for more personalized, risk-adapted screening strategies.

Interval Cancer Detection with AI (Dec 1, 11:30 AM–12:00 PM CST)

Prof. Fiona Gilbert (University of Cambridge) will present new evidence on the ability of AI to identify interval breast cancers typically missed during routine screening, outlining how AI-supported detection could reduce missed cancers and improve population-level screening outcomes.

Academic Leadership in AI Adoption (Dec 2, 10:30–11:00 AM CST)

Drs. Liz Morris (UC Davis Health) and Elizabeth Burnside (University of Wisconsin–Madison) will compare two distinct approaches to implementing breast AI in academic environments. The session will examine evidence, ethics, and practical considerations for responsible adoption.

Real-World DBT Performance (Dec 2, 4:30–5:00 PM CST)

Dr. Manisha Bahl (Mass General) will share new clinical data on how Lunit INSIGHT DBT performs in digital breast tomosynthesis workflows, highlighting improvements in cancer detection, diagnostic consistency, and the potential to reduce interval cancer rates when integrated into routine practice.
"RSNA is where the field looks to understand whether AI is delivering measurable clinical value, and this year’s program reflects that momentum," said Brandon Suh, CEO of Lunit. "Across mammography, DBT, and density-driven risk modeling, our studies highlight how rigorously validated AI can enhance screening performance, support radiologists, and strengthen the foundation for risk-adapted care. We remain committed to generating evidence that drives responsible and meaningful adoption in clinical practice."

(Press release, Lunit, DEC 2, 2025, View Source [SID1234661061])