On September 18, 2026 mAbxience, a majority-owned company of Fresenius SE & Co. KGaA (XETR: FRE; OTCM: FSNUY) with partial ownership from Insud Pharma; and Sandoz (SIX: SDZ / OTCQX: SDZNY), the global leader in affordable medicines, reported a licensing, development, manufacturing and commercialization agreement for an emicizumab biosimilar candidate. The collaboration agreement combines mAbxience’s proven development and manufacturing capabilities with Sandoz’s global commercial reach, creating a pathway to broaden patient access to this potential high-quality biologic medicine worldwide.

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Under the terms of the agreement, mAbxience will be responsible for the development and manufacturing of the agreed biosimilar through its state-of-the-art GMP-approved facilities in Spain and Argentina, while Sandoz will hold exclusive commercialization rights globally, excluding Argentina, Uruguay, and Paraguay. The financial terms of the agreement remain confidential. The agreement highlights the growing attractiveness of mAbxience’s development and manufacturing platform as healthcare systems prepare for a significant wave of biologic medicines losing exclusivity over the coming years.

Emicizumab is a proposed biosimilar candidate development referencing Hemlibra (emicizumab), and is indicated for the treatment of hemophilia A and represents an estimated global reference market of approximately USD 5.7 billion.

Hemophilia A is a rare genetic disorder caused by insufficient or defective factor VIII, a key blood-clotting protein. As the most common form of hemophilia, it accounts for around 80% of all cases worldwide and continues to represent a significant unmet medical need for patients and healthcare systems.

Jurgen Van Broeck, Chief Executive Officer of mAbxience, said: "This agreement with Sandoz represents a significant recognition of mAbxience’s development and manufacturing platform and the expertise of our teams. This agreement combines our capabilities with Sandoz’s global biosimilars reach and provides a clear pathway to broaden access to treatment for patients living with hemophilia A. It also reinforces our strategy of combining world-class development and manufacturing capabilities with selected commercial partnerships that can help accelerate patient access to high-quality biologic medicines worldwide."

The agreement further reinforces mAbxience’s position as a global leader in biosimilars with development and manufacturing capabilities across complex biologics. The proposed emicizumab biosimilar candidate would expand mAbxience’s presence in rare diseases and complement its growing biosimilar pipeline, which spans oncology, immunology, bone diseases, and other specialty care areas.

(Press release, mAbxience, SEP 18, 2026, View Source [SID1234670948])

On September 18, 2026 Chugai Pharmaceutical Co., Ltd. (TOKYO: 4519) reported that it has obtained approval from the Ministry of Health, Labour and Welfare (MHLW) on September 10, 2026 for FoundationOneCDx Cancer Genomic Profile to be used as a companion diagnostic for Pfizer Japan Inc’s third-generation ALK inhibitor, LORBRENA tablets 25 mg and 100 mg (generic name: lorlatinib), which is approved for ALK fusion gene-positive non-small cell lung cancer (NSCLC).

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This approval enables the detection of ALK fusion genes using the FoundationOne CDx Cancer Genomic Profile to guide the decision to use lorlatinib for ALK fusion gene-positive NSCLC.

FoundationOne CDx Cancer Genomic Profile has continuously expanded its companion diagnostic capabilities, enabling a single comprehensive genomic profiling test to support treatment decisions for multiple medicines. With this approval, the availability of companion diagnostics for ALK fusion gene-positive NSCLC will be further expanded, which is expected to enhance patient access to appropriate treatment options.

As a leading company in oncology, Chugai is committed to realizing more advanced personalized healthcare in the oncology field and contributing to patients through the wider adoption of comprehensive genomic profiling.

Approval information The underlined and bolded part has been newly added.

Intended uses or indications

The product is used for comprehensive genomic profiling of tumor tissues in patients with solid cancers.
The product is used for detecting gene mutations and other alterations to support the assessment of drug indications listed in the table below.
Alterations Cancer type Relevant drugs
Activated EGFR alterations Non-small cell lung cancer (NSCLC) afatinib, erlotinib, gefitinib, osimertinib
EGFR exon 20 T790M alterations osimertinib
ALK fusion genes alectinib, crizotinib, ceritinib, brigatinib, lorlatinib
ROS1 fusion genes entrectinib
MET exon 14 skipping alterations capmatinib
BRAF V600E and V600K alterations Malignant melanoma dabrafenib, trametinib, vemurafenib, encorafenib, binimetinib
BRAF V600 alterations and BRAF fusion genes Glioma tovorafenib
ERBB2 copy number alterations (HER2 gene amplification positive) Breast cancer trastuzumab
AKT1 alterations capivasertib
PIK3CA alterations
PTEN alterations
KRAS/NRAS wild-type Colorectal cancer cetuximab, panitumumab
Microsatellite instability high nivolumab
Microsatellite instability high Solid tumors pembrolizumab
Tumor mutational burden high pembrolizumab
NTRK1/2/3 fusion genes entrectinib, larotrectinib, repotrectinib
RET fusion genes selpercatinib
ALK fusion genes alectinib
BRCA1/2 alterations Ovarian cancer olaparib
BRCA1/2 alterations Prostate cancer olaparib
FGFR2 fusion genes Biliary tract cancer pemigatinib
About FoundationOne CDx Cancer Genomic Profile
Developed by Foundation Medicine Inc., FoundationOne CDx Cancer Genomic Profile is a next-generation sequencing based in vitro diagnostic device for the detection of substitutions, insertion and deletion alterations, and copy number alterations in 324 genes and select gene rearrangements, as well as genomic signatures including microsatellite instability (MSI) and tumor mutational burden (TMB) using DNA isolated from formalin-fixed, paraffin-embedded (FFPE) tumor tissue specimens. The program is available as a companion diagnostic for multiple molecular-targeted drugs approved in Japan.

Trademarks used or mentioned in this release are protected by law.

(Press release, Chugai, SEP 18, 2026, View Source [SID1234670947])

On September 18, 2026 Astellas Pharma Inc. (TSE: 4503, President and CEO: Naoki Okamura, "Astellas") reported that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion recommending the approval of PADCEV (enfortumab vedotin), in combination with Keytruda (pembrolizumab), as neoadjuvant treatment (before surgery) and then continued after radical cystectomy (surgery) as adjuvant treatment, for adults with resectable muscle-invasive bladder cancer (MIBC) in the European Union (EU).

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The CHMP based its positive opinion on results from the Phase 3 EV-304 clinical trial (KEYNOTE-B15), in which perioperative (neoadjuvant and adjuvant) enfortumab vedotin plus pembrolizumab significantly improved Event-Free Survival (EFS) and Overall Survival (OS) compared to standard-of-care neoadjuvant gemcitabine and cisplatin chemotherapy in adults with MIBC who were cisplatin-eligible.

Moitreyee Chatterjee-Kishore, Ph.D., MBA, Executive Vice President and Head of Oncology Development, Astellas
"Nearly half of patients with MIBC see their cancer return within five years, even after receiving neoadjuvant gemcitabine and cisplatin chemotherapy. This positive CHMP opinion brings us closer to changing that for patients across Europe, based on the significant survival improvements seen with perioperative enfortumab vedotin plus pembrolizumab."

In the trial, perioperative enfortumab vedotin plus pembrolizumab reduced the risk of tumor recurrence, progression, or death by 47% (Hazard Ratio (HR) 0.53; CI, 95%, 0.41–0.70; 1-sided p<0.0001) and reduced the risk of death by 35% (HR 0.65; 95% CI, 0.48-0.89; 1-sided p=0.0029).1

The safety profile was consistent with the known profiles of the individual medicines, and no new safety signals were observed.1 Grade ≥3 adverse events due to any cause occurred in 75.7% of patients treated with perioperative enfortumab vedotin plus pembrolizumab compared to 67.2% of patients treated with neoadjuvant chemotherapy.1

Results from the trial were recently published in The New England Journal of Medicine.1

Bladder cancer affects an estimated 200,000 people in Europe each year, with the region reporting the highest global incidence rates – particularly in Southern and Western Europe.2,3 MIBC accounts for approximately 30% of bladder cancer cases and is an advanced, aggressive form of the disease, in which cancer cells have entered the muscle wall of the bladder – increasing the risk that the disease will spread to other parts of the body if not treated effectively.4

Enfortumab vedotin plus pembrolizumab was approved by the European Commission (EC) in June 2026 as neoadjuvant and adjuvant treatment for cisplatin-ineligible adults with resectable MIBC. Approval in this setting would extend that indication to cisplatin-eligible patients, collectively covering adults with resectable MIBC regardless of cisplatin eligibility.

The EC is expected to issue a final decision on the application for enfortumab vedotin plus pembrolizumab within approximately two months. If approved, the EC’s decision will apply to all 27 European Union member states, as well as Iceland, Liechtenstein and Norway.

Astellas has already reflected the impact of the CHMP’s opinion in its financial forecast for the current fiscal year ending March 31, 2027.

About PADCEV (enfortumab vedotin)
PADCEV (enfortumab vedotin) is a first-in-class antibody-drug conjugate (ADC) that is directed against Nectin-4, a protein located on the surface of cells and highly expressed in bladder cancer.5 Nonclinical data suggest the anticancer activity of enfortumab vedotin is due to its binding to Nectin-4-expressing cells, followed by the internalization and release of the anti-tumor agent monomethyl auristatin E (MMAE) into the cell, which result in the cell not reproducing (cell cycle arrest) and in programmed cell death (apoptosis).5

Enfortumab vedotin in combination with pembrolizumab or pembrolizumab and berahyaluronidase alfa-pmph is approved as neoadjuvant treatment and then continued after radical cystectomy as adjuvant treatment for adult patients with muscle-invasive bladder cancer (MIBC) regardless of eligibility for cisplatin-containing chemotherapy in the United States. In the European Union (EU), enfortumab vedotin in combination with pembrolizumab is approved as neoadjuvant treatment and then continued after radical cystectomy as adjuvant treatment for adult patients with resectable MIBC who are ineligible for cisplatin-based chemotherapy.

Additionally, enfortumab vedotin plus pembrolizumab is approved for the treatment of adult patients with locally advanced or metastatic urothelial cancer (la/mUC) regardless of cisplatin eligibility in the United States, Japan, and a number of other countries around the world. In the EU, the combination is approved for the treatment of adult patients with unresectable or metastatic urothelial cancer who are eligible for platinum-containing chemotherapy.

About the EV-304/KEYNOTE-B15 Trial
The EV-304 trial is an ongoing, open-label, randomized, controlled, Phase 3 study evaluating neoadjuvant and adjuvant enfortumab vedotin in combination with pembrolizumab versus neoadjuvant chemotherapy (gemcitabine and cisplatin) in patients with MIBC who are eligible for cisplatin-based chemotherapy. Patients were randomized to receive either neoadjuvant and adjuvant (before and after surgery) enfortumab vedotin in combination with pembrolizumab (arm A) or neoadjuvant chemotherapy (arm B). Curative-intent surgery (cystectomy) was performed in both arms. Enfortumab vedotin in combination with pembrolizumab was administered as a planned total of 9 cycles of enfortumab vedotin and 17 cycles of pembrolizumab, split before and after surgery.

The primary endpoint of this trial is EFS, defined as the time from randomization to the first occurrence of any of the following events: progression of disease that precludes RC or failure to undergo RC in participants with residual disease, gross residual disease left behind at the time of surgery, local or distant recurrence based on BICR or death due to any cause. Key secondary endpoints include OS and pCR rate. For more information on the global EV-304 trial, go to clinicaltrials.gov.

(Press release, Astellas, SEP 18, 2026, View Source [SID1234670920])

On September 17, 2026 Kincell Bio and Cellipont Bioservices reported the completion of their merger to form Kincellis Advanced Therapies (Kincellis), a U.S.-based contract development and manufacturing organization focused on cell therapies and other advanced modalities.

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Kincellis Advanced Therapies brings together Kincell’s depth in immune-cell technologies with Cellipont’s experience across stem cells, iPSCs, MSCs, dendritic cells, exosomes and emerging mRNA-enabled approaches. This combined scientific breadth enables Kincellis to support autologous and allogeneic therapies across a wide range of cell types and modalities — from early development through commercial supply — giving customers access to deeper technical expertise and more comprehensive solutions within one organization.

Together, the two companies have released more than 150 GMP batches for clients and are supporting 10 IND filings this year alone, experience that reflects not only scale, but a shared commitment to helping promising therapies reach patients.

Darren Head serves as CEO of Kincellis and brings an outstanding track record of building advanced therapies CDMOs over the last two decades. "Kincell and Cellipont are highly complementary in their science, facilities and the stages of development they serve. Together, we can offer customers broader expertise and a more connected path from process and analytical development through late-stage manufacturing, while maintaining the responsiveness and hands-on partnership that are essential in cell therapy," said Darren Head, Chief Executive Officer, Kincellis Advanced Therapies.

Kincellis operates approximately 140,000 square feet of development and manufacturing infrastructure across Gainesville, Florida; Research Triangle Park, North Carolina; and The Woodlands, Texas. The combined network includes 16 operational, qualified GMP manufacturing suites supporting programs from early development and clinical manufacturing through pivotal and commercial supply.

The three-site network provides customers with greater flexibility, capacity and continuity as programs advance, while enabling Kincellis to align programs with the technical teams and manufacturing capabilities best suited to their development stage and supply needs. The experienced operations team, comprising leaders from both organizations and more than 200 dedicated team members, will be led by Larry Pitcher, President of Kincellis Advanced Therapies, who said, "Our priorities are clear: maintain continuity for every customer, connect the strongest capabilities of both organizations and build a common platform that can scale with customer needs. This combination creates meaningful opportunities for our customers, our teams and the advanced-therapies industry."

The company will be supported by an experienced Board led by Mark Bamforth OBE, as Executive Chair, who said, "Kincellis brings together the expertise, infrastructure and experience needed to support advanced-therapy innovators as their programs grow from the clinic toward commercial supply. We are creating a stronger, more scalable partner built around the realities of advanced-therapy development and supply."

The equity financing for the transaction was led by NewSpring Capital with support from existing investors Kineticos Life Sciences, HealthQuest Capital and Great Point Partners, together with a debt facility provided by J.P. Morgan. William Blair & Company served as financial advisor to Cellipont Bioservices. Financial terms were not disclosed.

(Press release, Kincell Bio, SEP 17, 2026, View Source [SID1234671020])

On September 17, 2026 MIRA Pharmaceuticals, Inc. (NASDAQ: MIRA) ("MIRA" or the "Company"), a clinical-stage pharmaceutical company developing novel oral small-molecule therapeutics, reported that, following review and comments from the U.S. Food and Drug Administration (FDA), the Phase 2a protocol evaluating Ketamir-2 in chemotherapy-induced peripheral neuropathy (CIPN) has been submitted for Institutional Review Board (IRB) review at a leading cancer research institution.

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MIRA incorporated the FDA’s feedback into the protocol and is targeting site initiation in the first quarter of 2027, subject to completion of IRB review and other routine site activation requirements. The study represents Ketamir-2’s first clinical evaluation in patients with CIPN and is designed to generate initial efficacy and dose-response data while further characterizing safety and tolerability.

"We are entering an important stage for Ketamir-2 as we prepare to evaluate the drug for the first time in patients with persistent CIPN," said Erez Aminov, CEO of MIRA. "This marks the transition from establishing safety and pharmacokinetics in healthy volunteers to evaluating Ketamir-2’s potential therapeutic effect in patients."

About the Phase 2a Study

The randomized, double-blind, placebo-controlled, three-period crossover study will enroll adults with moderate-to-severe persistent CIPN. Participants will receive Ketamir-2 at 300 mg and 600 mg, as well as placebo, in a defined treatment sequence across three seven-day treatment periods separated by 13-day washout periods, allowing each participant to serve as their own control.

The study will evaluate the safety, tolerability, efficacy, and dose-response relationship of oral Ketamir-2, including its effect on post-chemotherapy neuropathic pain intensity. Additional assessments will evaluate CIPN-related symptoms and functional status, as well as potential central nervous system adverse effects.

The study builds on MIRA’s completed Phase 1 clinical program in healthy volunteers, in which Ketamir-2 demonstrated a favorable safety, tolerability, and pharmacokinetic profile, with no serious adverse events or dose-limiting toxicities reported. The Phase 2a study will be conducted under MIRA’s active Investigational New Drug (IND) application.

Addressing a Significant Unmet Need in Neuropathic Pain

CIPN is a painful and potentially persistent complication of certain commonly used chemotherapies that can continue long after cancer treatment has ended. Treatment options remain limited, and there are currently no FDA-approved therapies specifically indicated for CIPN. Existing treatment approaches offer limited options for managing painful CIPN, underscoring the need for new therapies specifically developed for this condition.

Ketamine has demonstrated analgesic activity in neuropathic pain through modulation of the NMDA receptor pathway, supporting the therapeutic relevance of this mechanism. However, its broader use as a chronic treatment can be constrained by intravenous administration, dissociative and other neuropsychiatric effects, monitoring requirements, and its Schedule III controlled-substance status.

Ketamir-2 is being developed as an oral NMDA receptor modulator designed to engage this therapeutically relevant pathway while potentially overcoming key limitations associated with ketamine. Ketamir-2 is orally administered; its Phase 1 pharmacokinetic profile supports once-daily dosing, and it is not classified as a controlled substance by the U.S. Drug Enforcement Administration (DEA).

"There is a strong scientific rationale for targeting NMDA receptor signaling in neuropathic pain," said Itzchak Angel, Ph.D., Chief Scientific Advisor of MIRA. "Ketamine has provided important clinical validation of this pathway, but its properties can limit its practicality for chronic use. Ketamir-2 was designed as an oral NMDA receptor modulator with high selectivity and a differentiated pharmacologic profile, and we believe this Phase 2a study will provide an important first opportunity to determine whether this profile can translate into meaningful pain reduction in patients with persistent CIPN."

While CIPN is the initial patient population being evaluated in Phase 2a, MIRA believes that positive clinical evidence in CIPN could support the evaluation of Ketamir-2 across additional neuropathic pain conditions where NMDA receptor signaling may play a role. The Company views CIPN as a potential clinical entry point into the broader neuropathic pain market.

October Scientific Presentation and BioJapan Participation

MIRA expects to present Ketamir-2 at the International Conference on Addiction and Psychiatry in Tokyo, Japan, on October 5–6, 2026, where an abstract titled "An Oral Selective NMDA Modulator for Chemotherapy-Induced Peripheral Neuropathy—Phase 1 Safety, Pharmacokinetics, and Clinical Development Update" has been accepted for oral presentation by Dr. Itzchak Angel, MIRA’s Chief Scientific Advisor.

MIRA also expects to participate in BioJapan in October as the Company continues licensing and strategic partnership discussions around Ketamir-2 and its broader pipeline.

About Ketamir-2

Ketamir-2 is MIRA Pharmaceuticals’ proprietary oral NMDA receptor modulator in clinical development for neuropathic pain. The compound is designed to selectively modulate the NMDA receptor PCP binding site with low binding affinity and limited off-target receptor activity.

MIRA holds exclusive worldwide rights to Ketamir-2 and is pursuing intellectual property protection across major global pharmaceutical markets.

(Press release, Mira Pharmaceuticals, SEP 17, 2026, View Source [SID1234670943])