Chemomab Therapeutics to Present at H.C. Wainwright 27th Annual Global Investor Conference

On August 21, 2025 Chemomab Therapeutics Ltd. (Nasdaq: CMMB) (Chemomab), a clinical stage biotechnology company developing innovative therapeutics for fibro-inflammatory diseases with high unmet need, reported that Chief Executive Officer Dr. Adi Mor will deliver a corporate presentation at the H.C. Wainwright 27th Annual Global Investment Conference (Press release, Chemomab, AUG 21, 2025, View Source [SID1234655421]). Dr. Mor’s prerecorded presentation will be webcast and will be available starting on September 5, 2025 at 7:00 am ET. The link to access the webcast is included below and is also available at the Events section of the Chemomab website. Chemomab management will also be hosting 1×1 investor meetings during the conference on September 8 and September 9, 2025.

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Chemomab Presentation at H.C. Wainwright 27th Annual Global Investment Conference

Date: September 5, 2025
Time: Available starting at 7:00 am ET for 90 days
Venue: Virtual
Format: Prerecorded webcast presentation
Webcast Link: View Source

BioDlink’s Bevacizumab Approved for Market Launch in Indonesia, Marking Fourth Consecutive Emerging Market Authorization

On August 21, 2025 BioDlink reported that its Bevacizumab Injection has obtained marketing authorization from Indonesia’s National Agency of Drug and Food Control (BPOM) (Press release, BioDlink, AUG 21, 2025, View Source [SID1234655437]). This marks BioDlink’s fourth international approval within two months – following Nigeria, Pakistan, and Colombia – signaling accelerated BioDlink’s global expansion into a sustained commercialization phase.

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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Strategic Significance of Indonesian Approval
Indonesia, the world’s fourth-most populous nation, reports over 400,000 new cancer cases annually (WHO). Yet biologics accessibility remains below 15%. As ASEAN’s largest pharmaceutical market and regulatory hub, this approval expedites regional market access across Southeast Asia. BioDlink’s cost-effective bevacizumab, manufactured in China in compliance with international GMP standards, is helping to address critical treatment gaps for patients in Indonesia.

Global Standards, Proven Quality & Compliance
BPOM’s rigorous review process, fully aligned with PIC/S international standards, reinforces the clinical value of bevacizumab while reaffirming BioDlink’s world-class quality systems. Our manufacturing facility is GMP-certified across multiple regions—including China, Brazil, Egypt, Indonesia, Colombia, Argentina, and Pakistan—and recognized by Japan’s PMDA. This comprehensive accreditation ensures end-to-end compliance for antibodies, ADCs/XDCs, and biosimilar products.

This approval has proven BioDlink’s mature global commercialization capabilities:

Manufacturing Scale: Four commercial-scale manufacturing lines at the Suzhou site ensure a reliable global supply of antibodies, ADCs/XDCs, and biosimilars.
Regulatory Excellence: BPOM’s PIC/S-aligned approval stands as a global benchmark, underscoring the strength of BioDlink’s quality systems.
Strategic Momentum: Successive approvals across four markets are driving accelerated expansion in Southeast Asia and Latin America.
Dr. Jun Liu, Chief Executive Officer and Executive Director of BioDlink, stated:
"These consecutive approvals demonstrate the strength of our quality systems and commercial execution. With Indonesia as a key ASEAN hub, and in close partnership with Kexing Biopharm, we are shifting from single-market breakthroughs to regional impact —expanding access, diversifying growth, and delivering affordable, high-quality therapies worldwide."

Delcath Systems to Participate in Upcoming Investor Conferences

On August 21, 2025 Delcath Systems, Inc. (Nasdaq: DCTH), an interventional oncology company focused on the treatment of primary and metastatic cancers of the liver, reported that management will be attending the following investor conferences (Press release, Delcath Systems, AUG 21, 2025, View Source [SID1234655422]):

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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Wells Fargo Healthcare Conference on Thursday, September 4, 2025, in Boston, MA
H.C. Wainwright 27th Annual Global Investment Conference on Tuesday, September 9, 2025, in New York, NY

BioDlink’s Bevacizumab Approved for Market Launch in Indonesia, Marking Fourth Consecutive Emerging Market Authorization

On August 21, 2025 BioDlink reported that its Bevacizumab Injection has obtained marketing authorization from Indonesia’s National Agency of Drug and Food Control (BPOM) (Press release, BioDlink, AUG 21, 2025, View Source [SID1234655437]). This marks BioDlink’s fourth international approval within two months – following Nigeria, Pakistan, and Colombia – signaling accelerated BioDlink’s global expansion into a sustained commercialization phase.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Strategic Significance of Indonesian Approval
Indonesia, the world’s fourth-most populous nation, reports over 400,000 new cancer cases annually (WHO). Yet biologics accessibility remains below 15%. As ASEAN’s largest pharmaceutical market and regulatory hub, this approval expedites regional market access across Southeast Asia. BioDlink’s cost-effective bevacizumab, manufactured in China in compliance with international GMP standards, is helping to address critical treatment gaps for patients in Indonesia.

Global Standards, Proven Quality & Compliance
BPOM’s rigorous review process, fully aligned with PIC/S international standards, reinforces the clinical value of bevacizumab while reaffirming BioDlink’s world-class quality systems. Our manufacturing facility is GMP-certified across multiple regions—including China, Brazil, Egypt, Indonesia, Colombia, Argentina, and Pakistan—and recognized by Japan’s PMDA. This comprehensive accreditation ensures end-to-end compliance for antibodies, ADCs/XDCs, and biosimilar products.

This approval has proven BioDlink’s mature global commercialization capabilities:

Manufacturing Scale: Four commercial-scale manufacturing lines at the Suzhou site ensure a reliable global supply of antibodies, ADCs/XDCs, and biosimilars.
Regulatory Excellence: BPOM’s PIC/S-aligned approval stands as a global benchmark, underscoring the strength of BioDlink’s quality systems.
Strategic Momentum: Successive approvals across four markets are driving accelerated expansion in Southeast Asia and Latin America.
Dr. Jun Liu, Chief Executive Officer and Executive Director of BioDlink, stated:
"These consecutive approvals demonstrate the strength of our quality systems and commercial execution. With Indonesia as a key ASEAN hub, and in close partnership with Kexing Biopharm, we are shifting from single-market breakthroughs to regional impact —expanding access, diversifying growth, and delivering affordable, high-quality therapies worldwide."

Immuneering Announces $25 Million Private Placement

On August 21, 2025 Immuneering Corporation (Nasdaq: IMRX), a clinical-stage oncology company focused on keeping cancer patients alive, reported that it has entered into a definitive securities purchase agreement for a private placement of securities to top-tier institutional and other accredited investors, that is expected to result in up front gross proceeds to the Company of approximately $25 million, before deducting fees and expenses (Press release, Immuneering, AUG 21, 2025, View Source [SID1234655423]). The closing of the private placement is subject to customary closing conditions and is expected to occur on or about August 26, 2025.

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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"We are excited to announce updated Overall Survival (OS) and Progression-Free Survival (PFS) data from our ongoing Phase 2a trial of atebimetinib in combination with mGnP in first-line pancreatic cancer patients, planned in the coming weeks. In June, we reported an exceptional 94% OS observed at 6 months in first-line pancreatic cancer patients treated with atebimetinib in combination with mGnP. To put that in perspective, in the pivotal study of standard of care GnP, the 6-month OS was only 67%, and dropped rapidly to only 50% by 8.5 months," said Ben Zeskind, Ph.D., Co-founder and Chief Executive Officer of Immuneering. "Our exceptional 6-month overall survival data in first-line pancreatic cancer patients generated strong interest from leading pharmaceutical companies and top-tier investors, including the visionary investors participating in today’s financing. We are developing an entirely new category of cancer medicines, Deep Cyclic Inhibitors, which we believe represent an important new way to keep cancer patients alive and help them thrive. The proceeds from this financing will help support our ongoing efforts to bring atebimetinib, our Deep Cyclic Inhibitor of MEK in the MAPK pathway, to as many cancer patients as possible as quickly as possible."

Under the securities purchase agreement, the investors agreed to purchase: (i) an aggregate of 6,329,113 unregistered shares of the company’s Class A common stock at a purchase price of $3.95 per share (or, for certain investors in lieu of Class A common stock, pre-funded warrants to purchase shares of Class A common stock), and (ii) accompanying purchase warrants to purchase an aggregate of 2,848,096 shares of Class A common stock, with each such warrant representing the right to purchase one share of the company’s Class A common stock at an exercise price of $5.50 per share. The pre-funded warrants were issued for a purchase price equating to $3.949 per pre-funded warrant share (which was the per share purchase price for the Class A common stock less the $0.001 per share unfunded exercise price for each pre-funded warrant). The $3.95 per share purchase price for the Company’s Class A common stock represents a premium of approximately 15% as compared to the Company’s last reported closing price on August 20, 2025. The investors will be granted registration rights as part of the transaction. The purchase warrants will be exercisable for a period of five years following the date on which the Class A common stock issued and issuable in the transaction are registered for resale.

The offer and sale of the foregoing securities are being made in a transaction not involving a public offering and the securities have not been registered under the Securities Act of 1933, as amended (the "Securities Act"), or applicable state securities laws. Accordingly, the securities may not be reoffered or resold in the United States except pursuant to an effective registration statement or an applicable exemption from the registration requirements of the Securities Act and such applicable state securities laws.

This press release does not constitute an offer to sell or the solicitation of an offer to buy the securities, nor shall there be any sale of the 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 such state or other jurisdiction.