SL Science Presents Preclinical Data at the 85th Annual Meeting of the Japanese Cancer Association Showing γδ T Cells Target Chemotherapy-Resistant Glioblastoma

On September 24, 2026 SL Science Holding Limited ("SL Science" or the "Company") (NASDAQ: SLBT), a Taiwan-headquartered biomedical company specializing in developing innovative cellular and gene therapies, reported new preclinical data evaluating unmodified human γδ T cells in glioblastoma (GBM) — the Company’s unmodified γδ T cell therapy platform (the "GDT platform"). The findings are being presented as poster P-2017 at the 85th Annual Meeting of the Japanese Cancer Association, held from September 24–26, 2026. The research was conducted in collaboration with investigators at Taipei Medical University (TMU), JY BioMed, and HeXun Biosciences.

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Key Data Presented
Targeting Resistant Cells: In advanced laboratory models, γδ T cells showed preferential cytotoxicity toward O6-methylguanine-DNA methyltransferase (MGMT)-positive GBM cells, which are typically resistant to standard chemotherapy.

Rapid Tumor Elimination: Real-time analysis across three distinct GBM cell lines (U87MG, T98G, and LN229) showed a dose-dependent drop in tumor cells upon the addition of γδ T cells.

Superior Efficacy: The γδ T cells exhibited higher cancer-killing activity than conventional αβ T cells in direct in vitro comparisons.

In Vivo Survival: Contextual data confirmed that the therapy reduced tumor size and prolonged survival in an intracranial GBM model, without obvious tolerability issues or macroscopic adverse findings.

Overcoming Standard Chemotherapy Limits
Glioblastoma is traditionally treated with surgery, radiotherapy, and the chemotherapy drug temozolomide. However, tumors reliably return. A key driver of this recurrence is the MGMT repair enzyme: cancer cells expressing this enzyme can reverse the DNA damage caused by chemotherapy, allowing them to survive treatment.

The new data show that SL Science’s γδ T cells directly address this chemo-resistant population. Because γδ T cells recognize general stress signals on cancer cells rather than relying on a single antigen, their cancer-killing ability is not hindered by the tumor’s DNA-repair mechanisms. In short, the cells are active against the exact fraction of the tumor that standard chemotherapy struggles to eliminate.

A Clear Development Pathway
This presentation marks the third recent milestone in a defined development sequence for the Company. It follows a July presentation in Melbourne demonstrating the therapy’s ability to control tumor growth in vivo, and an August peer-reviewed publication outlining the clinical development requirements for this modality. The current data helps answer a crucial third question: identifying which patients and tumor types are suited for this approach.

"Showing that something kills tumor cells is the beginning of the work, not the end of it," said Mr. William Wang, Chairman and Chief Executive Officer of SL Science. "What we are presenting in Japan is a highly practical result: these cells appear active against the MGMT-positive fraction, which is the fraction temozolomide leaves behind. If that holds up, it tells us where this therapy belongs in the treatment sequence and which patients it is matched to. These remain preclinical findings, and we are presenting them where they can be rigorously examined by the field."

(Press release, SL Science, SEP 24, 2026, View Source [SID1234671048])

The United Kingdom approves Zepzelca® (lurbinectedin) by PharmaMar in combination with atezolizumab for first-line maintenance treatment of small cell lung cancer

On September 24, 2026 PharmaMar (MSE: PHM) reported that the Medicines and Healthcare products Regulatory Agency (MHRA) has granted approval in the United Kingdom for Zepzelca (lurbinectedin) in combination with atezolizumab (Tecentriq) as a first-line maintenance treatment for adults with extensive-stage small cell lung cancer (ES-SCLC), whose disease has not progressed following first-line induction therapy with atezolizumab, carboplatin, and etoposide.

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This approval is based on the results of the Phase III IMforte trial.[1]

According to the National Lung Cancer Audit (NLCA), 37,750 people were diagnosed with lung cancer in England only in 2023. Since small cell lung cancer (SCLC) accounts for approximately 15% of all lung cancer cases, this would correspond to roughly to 5,700 SCLC cases annually[2].

With this authorization, the United Kingdom joins the list of the territories where this combination has been approved, bringing the total number to 21, including the European Union (EU) and the United States.

(Press release, PharmaMar, SEP 24, 2026, View Source [SID1234671047])

HCW Biologics Inc. Announces Pricing of $1.5 Million Private Placement

On September 24, 2026 HCW Biologics Inc. (the "Company" or "HCW Biologics"), (NASDAQ: HCWB), a clinical-stage biopharmaceutical company developing transformative fusion immunotherapeutics to treat autoimmune diseases, cancer and senescence-associated dysplasia, reported the pricing of its $1.5 million private placement (the "Offering") with an existing stockholder of the Company, (the "Investor"). Pursuant to a securities purchase agreement entered into on September 23, 2026 with the Investor (the "Purchase Agreement"), the Company agreed to issue and sell an aggregate of 903,614 units (the "Units"), with each Unit consisting of (i) one pre-funded warrant (a "Pre-Funded Warrant") to purchase one share of the Company’s common stock, par value $0.0001 per share, ("Common Stock") and (ii) the right to receive one common stock purchase warrant (a "Common Warrant") to purchase one share of Common Stock, and subject to, stockholder approval of the issuance thereof.

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In connection with the Offering, the Company will issue 903,614 Pre-Funded Warrants. Subject to stockholder approval, which the Company is obligated to seek pursuant to the terms of the Purchase Agreement, the Investor will also be entitled to receive Common Warrants to purchase up to an aggregate of 903,614 shares of Common Stock.

Maxim Group LLC is acting as the sole placement agent for the Offering.

The combined purchase price for each Unit consisting of a Pre-Funded Warrant and the right to receive one Common Warrant upon, and subject to, stockholder approval of the issuance thereof, was $1.6599 per Unit. The Pre-Funded Warrants have an exercise price of $0.0001 per share of Common Stock, are exercisable immediately and will not expire until exercised in full. The Common Warrants will have an exercise price of $1.66 per share and will expire on the five and one half (5.5) year anniversary of their issuance. Under Nasdaq Listing Rule 5635(d), the Company is required to obtain stockholder approval before issuing the Common Warrants because the potential issuance of shares upon exercise of the Common Warrants could exceed the thresholds set forth in such rule. Following receipt of stockholder approval, the Company will issue the Common Warrants to the Investor in accordance with the Purchase Agreement.

The Company intends to use the net proceeds from this Offering to continue clinical trials for HCW9302, advance its IND-enabling studies for its T-Cell Engager, HCW11-018b, and its second-generation immune checkpoint inhibitor, HCW11-040, and for general corporate purposes.

On September 23, 2026, the Company also entered into a registration rights agreement with the Investors, pursuant to which the Company agreed to submit to the U.S. Securities and Exchange Commission (the "SEC") a registration statement on Form S-1 within 15 trading days of the closing of the Offering covering the resale of the shares of Common Stock issuable upon exercise of the Pre-Funded Warrants and the shares of Common Stock issuable upon exercise of the Common Warrants. The Company also agreed to use commercially reasonable efforts to cause the registration statement to be declared effective by the SEC within 60 days following the closing of the Offering.

The number of shares of Common Stock the Company that may be held by the Investor, including those shares issued at closing and upon the exercise of Pre-Funded Warrants from time to time in the Offering, may not exceed 9.99% of the number of shares of the Company’s Common Stock outstanding immediately after giving effect to such issuances.

This press release shall not constitute an offer to sell or a solicitation of an offer to buy any of the securities described herein, nor shall there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such state or other jurisdiction.

(Press release, HCW Biologics, SEP 24, 2026, View Source [SID1234671046])

Grant of Restricted Stock Units and Warrants to Employees in Genmab

On September 24, 2026 Genmab A/S (Nasdaq: GMAB) reported that the Board of Directors decided to grant 13,794 restricted stock units and 13,331 warrants to employees of the Company and the Company’s subsidiaries.

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Each restricted stock unit is awarded cost-free and provides the owner with a conditional right to receive one share in Genmab A/S of nominally DKK 1. The fair value of each restricted stock unit is equal to the closing market price on the date of grant of one Genmab A/S share, DKK 2,268.

The restricted stock units will vest on the first banking day of the month following a period of three years from the date of grant. Furthermore, the restricted stock units are subject to vesting conditions set out in the restricted stock unit program adopted by the Board of Directors. Information concerning Genmab’s restricted stock unit program can be found on www.genmab.com under Investors > Governance > Compensation > Restricted Stock Units.

The exercise price for each warrant is DKK 2,268. Each warrant is awarded cost-free and entitles the owner to subscribe one share of nominally DKK 1 subject to payment of the exercise price. By application of the Black-Scholes formula, the fair value of each warrant can be calculated as DKK 781.96.

The warrants vest three years after the grant date, and all warrants expire at the seventh anniversary of the grant date. The new warrants have been granted on the terms and conditions set out in the warrant program adopted by the Board of Directors on February 23, 2021. Information concerning Genmab’s warrant schemes can be found on www.genmab.com under Investors > Governance > Compensation > Warrants.

(Press release, Genmab, SEP 24, 2026, View Source [SID1234671045])

Cullinan Therapeutics Highlights Fourth Quarter 2026 Milestones Across Immunology and Oncology T Cell Engager Portfolio

On September 24, 2026 Cullinan Therapeutics, Inc. (Nasdaq: CGEM; "Cullinan"), a clinical-stage biopharmaceutical company accelerating potential first- or best-in-class, disease-modifying T cell engagers in autoimmune diseases and cancer, reported fourth quarter 2026 milestones across its immunology and oncology pipeline.

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"We look forward to providing several updates across our T cell engager programs in the fourth quarter of 2026. Starting with autoimmune diseases, for CLN-978 we look forward to sharing the most comprehensive clinical data set to date for a CD19 T cell engager across all indications, with multi-dose regimen data reported concurrently for SLE, RA, and now Sjögren’s disease also. For velinotamig, we will provide multi-dose regimen data from the ongoing Phase 1 dose escalation study as we advance the program in plasma cell driven diseases. Together, our CD19- and BCMA-targeted programs reflect a differentiated approach to treating autoimmune diseases, aiming to address distinct disease drivers across a broad range of conditions. For CLN-049, we plan to provide an update with longer follow up from the dose escalation portion of our ongoing Phase 1 study in a broad, all-comer population of relapsed/refractory AML patients. We look forward to rapidly progressing this program and initiating our potentially registrational Phase 2 study, following our recent successful meeting with the FDA," said Nadim Ahmed, President and CEO of Cullinan Therapeutics.

The Company plans to share the following immunology and oncology pipeline updates in Q4 2026:

•
CLN-978 (CD19xCD3 T cell engager): treatment-refractory moderate to severe systemic lupus erythematosus (SLE), difficult-to-treat rheumatoid arthritis (RA), and treatment-refractory moderate to severe Sjögren’s disease (SjD)
o
Multi-dose and single target dose regimen data in SLE, RA, and SjD in December
•
Velinotamig (BCMAxCD3 T cell engager): treatment-refractory autoimmune diseases driven by long-lived plasma cells
o
Multi-dose regimen data from the ongoing Genrix Bio Phase 1 dose escalation study in SLE to be shared in poster session at ACR Convergence 2026 on November 8, 2026, 10:30 a.m. to 12:30 p.m. ET

•
CLN-049 (FLT3xCD3 T cell engager): relapsed/refractory acute myeloid leukemia (AML)
o
Updated data from the dose escalation portion of the Phase 1 study in December

(Press release, Cullinan Oncology, SEP 24, 2026, View Source [SID1234671044])