Nurix Therapeutics to Participate in Upcoming Investor Conferences

On October 30, 2025 Nurix Therapeutics, Inc. (Nasdaq: NRIX), a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of targeted protein degradation medicines, reported that Arthur T. Sands, M.D., Ph.D., president and chief executive officer of Nurix, will participate in fireside chats at the following investor conferences in November.

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!

Stifel 2025 Healthcare Conference, New York, NY
Thursday, November 13, 2025, from 9:20 – 9:50 a.m. ET
Jefferies Global Healthcare Conference – London, UK
Wednesday, November 19, 2025, from 11:00 – 11:25 a.m. GMT
The fireside chats will be webcast live and can be accessed via a link in the Investors section of the Nurix website. The archived webcasts will be available for 30 days after the event.

(Press release, Nurix Therapeutics, OCT 30, 2025, View Source [SID1234657168])

Syndax Announces Participation in November Investor Conferences

On October 30, 2025 Syndax Pharmaceuticals (Nasdaq: SNDX), a commercial-stage biopharmaceutical company advancing innovative cancer therapies, reported that Michael A. Metzger, Chief Executive Officer, as well as members of the Syndax management team, will participate in the following upcoming investor conferences:

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!

UBS Global Healthcare Conference 2025 with a fireside chat on Monday, November 10, 2025, at 11:00 a.m. ET.
Guggenheim Second Annual Healthcare Innovation Conference with a fireside chat on Tuesday, November 11, 2025, at 3:00 p.m. ET.
Stifel 2025 Healthcare Conference with a fireside chat on Thursday, November 13, 2025, at 10:00 a.m. ET.
Jefferies 2025 London Healthcare Conference with a fireside chat on Thursday, November 20, 2025, at 10:00 a.m. GMT/ 5:00 a.m. ET.
A live webcast of the fireside chats will be available in the Investor section of the Company’s website at www.syndax.com, where a replay will also be available for a limited time.

(Press release, Syndax, OCT 30, 2025, View Source [SID1234657166])

REGiMMUNE presented preclinical data of recent development of its antibody program at Antibody Engineering & Therapeutics Asia 2025 in Kyoto, Japan

On October 30, 2025 REGiMMUNE Limited ("REGiMMUNE" or "the Company"), a clinical stage biopharma company developing novel immune therapeutics targeting regulatory T cells (Treg), reported preclinical data of its antibody program at the meeting of Antibody Engineering & Therapeutics Asia 2025 in Kyoto, Japan from Oct. 20 – 22.

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!

REGiMMUNE, while pursuing RGI-2001 in advanced clinical development for (Graft vs Host Disease (GvHD), armed with our long-time expertise in human immunology and Treg cells, has been actively developing its therapeutic antibody program. This pipeline currently includes RGI-6004 and AB01, both targeting tumor infiltrating Treg cells, reflecting the two strategies of therapeutic modulation of Treg cells, namely, depleting vs silencing, and AB08-H1 targeting a surface marker shared by blood-borne and solid malignancies.

The presentation in Kyoto included RGI-6004 and AB08-H1. RGI-6004 was developed to highly selectively target tumor infiltrating Treg cells while maintaining all other immune effector cells intact to alleviate the immune suppression in the tumor microenvironment, and consequently enhance anti-cancer immunity. AB08-H1 is an antibody developed to kill malignant cells of Hodgkin & Non-Hodgkin diseases and solid cancer cells via a unique target.

RGI-6004, an Afucosylated Antibody to Target GARP/LAP-TGFβ1 for Selective Depletion of Activated Tregs. RGI-6004, a fully human IgG1 against GARP/Latent-TGFb1 complex, designed to deplete tumor infiltrating activated Treg cells. The antibody specifically binds to activated human Treg cells with high affinity, but none to non-activated Treg cells, and CD4+ and CD8+ T effector cells. The antibody recognizes tumor infiltrating Treg cells in clinical solid tumor tissues. Its afucosylated version highly selectively depletes activated Treg cells with a significantly enhanced efficacy of ~10 pM, but none of CD4+ and CD8+ effector T cells, while granzyme B induction & proliferation of CD4+ and CD8+ effector T cells are not affected. RGI-6004 has minimal impact on platelets (counts and degranulation), minimal binding to major immune cells, nor observable impact on hematological profile of normal human blood. In cynomolgus monkey, its t1/2 is shown to be ~10 days, while its clinical hematology, coagulation, blood chemistry, immunophenotyping in peripheral blood, serum cytokine analysis, and pathology, does not demonstrate safety alarms. In sum, the behavior of RGI-6004 highlights the potential as a next-generation Treg-depleting agent in cancer immunotherapy.

AB08-H1, A humanized antibody that directly kills cancer target cells without ADCC and CDC. AB08-H1 is a humanized IgG that specifically targets pan MHC II (synonym for HLA II, human leukocyte antigen). Upon binding to the cell surface MHC class II molecule, the antibody induces homotypic aggregation, lysosomal membrane permeabilization, and ultimately cell lysis of the target malignant cells directly without the involvement of ADCC and CDC. REGiMMUNE overcame the original bottleneck of protein production of the humanized IgG, developed a high yield method to manufacture it in mammalian cells. As MHC Class II molecules are found highly expressed on lymphoid malignant cells, and have been increasingly recognized to express highly in major solid cancer cells, AB08-H1 is expected to treat various types of lymphoid malignancies (Hodgkin and Non-Hodgkin lymphomas), and solid cancers.

REGiMMUNE is encouraged by the recent news of Nobel Prize in Physiology granted to Dr. Shimon Sakaguchi and others, for their works on Treg cells. We are pleased to see that the fundamental roles of Treg cells in autoimmune disease, GvHD, cancer, and infectious disease are recognized in highest profile. REGiMMUNE is committed to developing therapeutics with, as Dr. Shimon Sakaguchi well put it, Treg-up strategies vs Treg-down strategies.

(Press release, REGimmune, OCT 30, 2025, View Source [SID1234657165])

PharmaMar Group Announces Financial Results as of September 30th, 2025

On October 30, 2025 PharmaMar Group (MSE: PHM) reported a 3% increase in total revenue during the first nine months of this year, reaching €130.9 million. Recurring revenue, resulting from the sum of net sales plus royalties received from our partners, grew by 6% to €105.6 million as of September 30th, 2025.

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!

As of September 30th this year, total sales in oncology amounted to €62.4 million, representing a 9% increase over the same period last year. These sales include commercial sales of Yondelis (trabectedin) in Europe, sales of raw materials to our partners, both trabectedin and lurbinectedin, and the positive performance of Zepzelca (lurbinectedin) in Europe, whose revenues increased by 34.7% in the first nine months of this year, reaching €31.4 million. Of particular note are revenues from lurbinectedin under the compassionate use program—mainly in France—which increased by 22% to €21.8 million, and commercial sales of Zepzelca in Switzerland, which amounted to €9.6 million, representing growth of 76% compared to the same period in 2024.

As of September 30th, 2025, oncology royalty income grew by 2% to €43.2 million. This amount corresponds mainly to royalties received from sales of lurbinectedin by our partners Jazz Pharmaceuticals and Luye Pharma, which together amounted to €35.0 million[1].. Added to this amount are royalties from sales of trabectedin by our partners in the US and Japan, totaling €8.2 million.

Non-recurring income from licensing agreements amounted to €25.3 million at the end of the first nine months of 2025, compared to €26.9 million in the same period last year. Noteworthy is the lurbinectedin licensing agreement for Japan signed with Merck for €21.0 million in April 2025, together with €3.0 million in deferred revenue from the 2019 agreement signed with Jazz Pharmaceuticals in relation to lurbinectedin. In the current fiscal year, the annual revenue recognition for the latter agreement is estimated at €4 million, while the total amount to be recognized in the previous fiscal year was approximately €23 million. Of the total €300 million in revenue received in 2020 in relation to the agreement signed with Jazz Pharmaceuticals, 94% of the total has been recognized in the income statement.

PharmaMar group’s investment in R&D stood at €69.6 million as of September 30, compared to €75.98 million for the first nine months of the previous year.

Of the total R&D investment for the period, the oncology segment recorded €66.0 million, compared to €70.0 million as of September 30, 2024. This variation is mainly due to the completion, in December 2024, of recruitment for the LAGOON Phase III clinical trial with lurbinectedin in small cell lung cancer.

The Company continues to invest in the clinical development of other molecules in earlier Phase I stages with PM534 and PM54, all for the treatment of solid tumors.

The RNAi segment recorded €3.6 million in R&D as of September 30, 2025, compared to €6.0 million in the same period of the previous year. This variation is due to the completion in the first months of 2024 of the PIVO1 Phase III clinical trial with tivanisiran for dry eye.

As of September 30th, 2025, the Group’s EBITDA reached €23.1 million, compared to €6.3 million in the same period of the previous year.

As a result of all the above, the PharmaMar Group doubled its net profit compared to the same period last year, reaching €15.3 million vs. €7.4 million.

(Press release, PharmaMar, OCT 30, 2025, View Source [SID1234657164])

Olema Oncology to Present Trial-in-Progress Poster for Phase 3 OPERA-02 Trial of Palazestrant Plus Ribociclib at SABCS 2025

On October 30, 2025 Olema Pharmaceuticals, Inc. ("Olema" or "Olema Oncology", Nasdaq: OLMA), a clinical-stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted therapies for breast cancer and beyond, reported it will present a trial-in-progress poster for the Phase 3 OPERA-02 trial at the 2025 San Antonio Breast Cancer Symposium (SABCS 2025) taking place December 9-12, 2025 in San Antonio, TX. The trial is evaluating palazestrant in combination with ribociclib in frontline estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-) advanced or metastatic breast cancer.

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!

Poster Presentation Details
Title: OPERA-02: a phase 3 randomized, double-blind, active-controlled study of palazestrant with ribociclib versus letrozole with ribociclib for the first-line treatment of ER+, HER2- advanced breast cancer
Abstract Number: 264
Presentation Number: PS5-12-18
Date/Time: Friday, December 12, 2025 from 12:30pm–2:00pm CT / 1:30pm–3:00pm ET

Additional information can be found on the SABCS website. A copy of the poster will be made available on the Publications page of Olema’s website in alignment with the SABCS 2025 embargo policy.

(Press release, Olema Oncology, OCT 30, 2025, View Source [SID1234657163])