Italfarmaco acquires 100% of Lacer, a Spanish pharmaceutical company that is a leader in health care and personal hygiene

On July 24, 2022 Italfarmaco, an Italian multinational company in the chemical-pharmaceutical sector, reported that it has acquired 100% of Lacer Pharmaceuticals, one of the leading companies in Spain in the area of health and personal hygiene (Press release, Italfarmaco, JUL 24, 2022, View Source [SID1234616943]).

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With an experience of over 70 years, a turnover in 2021 of over 150 million euros and almost 500 employees, Lacer is the market leader in practically all the areas in which it operates, in particular in the oral and dental sector with the Lacer brand, and brands such as Thrombocid, Pilexil, Anso and Talquistina. Lacer also has a broad portfolio of drugs in the cardiovascular and urogynecological sectors.

With this acquisition, Italfarmaco is strengthening its presence in the Spanish healthcare market, where it is already present with established brands, and is consolidating its current business areas in which it has been successfully operating for over 30 years in Italy and around the world. These include the thrombosis and critical ischemia sector, with brands such as Ghemaxan; gynecology with Natalben, Nuperal / Cariban and Ainara; and neurology and psychiatry sectors with brands such as Sonirem and Gliatilin. The Company recently achieved a major breakthrough with Givinostat, the first product that has been shown to be clinically significant in a Phase 3 study of patients with Duchenne muscular dystrophy (DMD), for which registration in the United States and Europe will be requested in the following months.

Furthermore, Italfarmaco, by incorporating the Lacer production plant in Cerdanyola del Valles, will add an important asset to the industrial activities of the Group which already has 5 production plants.

The integration into Italfarmaco will allow Lacer to consolidate its leading position in Spain, actively investing in existing brands and expanding its product portfolio, both in the healthcare sector and in the Prescription Medicines division. Furthermore, Lacer, benefiting from Italfarmaco’s global sales network of branches and distributors, will be able to increase its growth internationally.

Francesco De Santis, President of Italfarmaco, comments: "This acquisition represents a strong consolidation of our company in the Spanish market and represents a further impetus for our growth at international level. Lacer’s business, brands and our pool of talented people represent a strong element of continuity to Italfarmaco’s spirit of growth both in the areas where we are already present and in new therapeutic alternatives that can improve people’s health".

Lacer comments: "Lacer will benefit from the support of a new experienced partner that will allow both companies to grow towards the creation of a European pharmaceutical leader. This integration will allow Lacer to continue its success story and ensure that the legacy that started over 70 years ago will continue".

Qiming’s Portfolio Company InventisBio Lists on STAR Market

On July 24, 2022 Qiming Venture Partners’ portfolio company InventisBio (SHSE: 688382), a leading company in innovative drug development, reported that listed on the Science and Technology Innovation Board (the "STAR Market") of the Shanghai Stock Exchange (Press release, InventisBio, JUL 24, 2022, View Source [SID1234616892]). The issue price is CNY 18.12 per share, representing a market cap of CNY 10.419 billion.

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Qiming Venture Partners invested in InventisBio in September 2020. The successful listing of the company marks the fourth IPO in Qiming’s portfolio in 2022. InventisBio has become the ninth portfolio company listed on the STAR Market.

InventisBio is a China-based global biotech company dedicated to the research and development (R&D) of innovative drugs, with a focus on cancer, metabolic diseases and other major diseases. The company is co-founded by several professional experts with international backgrounds. InventisBio’s core R&D team members have an average of more than 20 years of experience in innovative drug R&D and team management in multinational pharmaceutical companies.

With strength and rich experience in drug R&D, InventisBio has independently developed a series of innovative targeted drugs with patent protection, covering non-small cell lung cancer (NSCLC), breast cancer, colorectal cancer and other solid tumors, as well as metabolic diseases such as hyperuricemia and gout.

InventisBio has business cooperation with well-known pharmaceutical enterprises including Betta Pharma, Pfizer, and Merck (MSD) among many others. Currently, with three core products at the clinical trial stage, five projects at the pre-clinical stage, and three core products entering phase II or phase III clinical registration trials, the company has been foremost among those who have made progress in drug R&D in China and even the world.

According to InventisBio, the company is committed to addressing unmet medical needs, developing innovative drugs with proprietary rights to be marketed worldwide, and consistently providing patients with safer, more effective and more affordable treatments. The successful listing on the STAR Market brings a new opportunity to InventisBio. The company will accelerate its product industrialization and commercialization, while continuing to enrich the product pipeline by advancing more candidate compounds into global clinical trial phases.

Dr. Kan Chen, Partner of Qiming Venture Partners, said, "Equipped with rich experience in innovative drug development, InventisBio’s team has profound insights into the industry trends. The company’s product pipeline has made progress to date. Many projects have entered the clinical stage or late-clinical stage and demonstrated best-in-class potential. The company’s IPO is a new starting point, and we look forward to InventisBio strengthening its industrialization and commercialization capability to better benefit patients with more of its products entering the late-clinical stage and obtaining approval to be marketed."

US FDA APPROVES QBIOTICS INVESTIGATIONAL NEW DRUG APPLICATION TO INITIATE TIGILANOL TIGLATE SOFT TISSUE SARCOMA PHASE II TRIAL

On July 24, 2022 QBiotics Group Limited (QBiotics), a life sciences company developing novel small molecule oncology and wound healing pharmaceuticals, reported that it has been granted approval of its Investigational New Drug (IND) application by the US Food and Drug Administration (FDA) for lead oncology molecule, tigilanol tiglate (Press release, QBiotics, JUL 24, 2022, View Source [SID1234616891]). The approval enables initiation of a Phase II clinical trial (QB46C-H07) in patients with STS.

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The QB46C-H07 trial will be undertaken in the USA. This is an open label study that will enrol at least 10 patients with advanced or metastatic STS. Patients will receive up to five intratumoural treatments of tigilanol tiglate, administered four weeks apart, to evaluate the drug candidate’s efficacy and safety in the treatment of STS.

Tigilanol tiglate is a plant-derived small molecule, administered by injection directly into a solid tumour. Injected tumours are rapidly destroyed by tumour cell necrosis, tumour vascular disruption, and immune-mediated mechanisms2.

Dr Victoria Gordon, Managing Director and CEO of QBiotics, said "IND approval for our Soft Tissue Sarcoma trial is an important milestone for QBiotics. It is QBiotics’ first FDA IND and the culmination of a very significant body of work by our team. IND approval is underpinned by a robust data package, including data from our first-in-human QBC46-H01 Phase I study, where tigilanol tiglate demonstrated clinically relevant monotherapy activity in 22 patients with a broad range of refractory solid tumours3."

"This STS trial builds on our overall development approach for tigilanol tiglate, which is exploring this drug candidate’s potential as a pan-tumour treatment for a broad range of solid tumours. QBiotics is also undertaking clinical trials in melanoma and head and neck cancer as part of this broad programme. Implementing a clinical trial in a third cancer indication is a strong move for the company."

"STS are a group of rare and heterogeneous solid tumours that occur in the soft tissues of the body, such as muscles and nerves," continued Dr Gordon. "Due to the complexity of this disease, treatment is challenging 4. We hope that through our research, we may be able to bring forward a new therapeutic option."

Global Data estimates that there were 124,573 new cases of STS globally in 2021, with the incidence growing at 0.54% per year1.

FURTHER

DR VICTORIA GORDON, CEO & MANAGING DIRECTOR, QBIOTICS GROUP

ABOUT TRIAL QB46C-H07
QB46C-H07 is a Phase II, open label clinical trial to evaluate the efficacy and safety of intratumoural tigilanol tiglate in 10 patients with advanced and/or metastatic Soft Tissue Sarcomas of the extremities and body wall.

Primary objective:
Evaluate the degree of tumour ablation in tumours and or tumour segments treated with one or more injections of tigilanol tiglate.

Secondary and exploratory objectives:
Safety and tolerability assessments of tigilanol tiglate, and translational research to evaluate changes in the tumour micro environment, immune responses, and tumour recurrence rate after 6 months following treatment.

Celluris participates in the Bioconvention 2022

On July 24, 2022 Celluris reported that participated this june in the largest biotechnology fair in World, the BioConvention in San Diego (Press release, (Press release, Celluris, JUL 24, 2022, View Source [SID1234616887]), JUL 24, 2022, View Source [SID1234616887]). These were intense days, with more than 30 meetings with industry players, such as related companies and innovation agents from other countries. In addition to the participation we made a presentation pitch on Brazilian Startup Day. Together with the Brazilian delegation in the event, there was the publication of the 6th edition of bioBr Magazine that was shared with everyone during the event and can be accessed digitally via the link to next: CLICK HERE In addition, Brazilian startups had a published article in Yahoo Finance : SEE HERE

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June 2022 Quarterly Activity Report

On July 22, 2022 Race Oncology reported that The June 2022 quarter (Q4 FY 2022) was highlighted by the successful completion of the Phase 1b stage of the relapsed or refractory Acute Myeloid Leukaemia (R/R AML) trial of Zantrene (bisantrene dihydrochloride) running at the Chaim Sheba Medical Centre, Israel (ASX announcement: 27 May 2022) (Press release, Race Oncology, JUL 22, 2022, View Source [SID1234617042]). Encouraging clinical responses were observed in a very heavily pre-treated AML patient population with 3 of the 6 patients bridged to a stem cell transplant. The study led by Professor Arnon Nagler now advances to the Phase 2 efficacy stage with the intention of recruiting up to 17 patients.

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A second highlight was the discovery that Zantrene protects the hearts of mice from the damaging effects of anthracyclines (specifically doxorubicin)-even when the chemotherapeutic dose was increased and without significant additional toxicity or bone marrow suppression (ASX announcement: 30 June 2022).

Our extramedullary AML clinical trial received all ethics and regulatory approvals and is expected to treat the first patient in the current quarter-Q3 CY 2022 (ASX announcements: 6 April 2022 and 12 May 2022). This is the first clinical trial in the world to investigate the targeting of FTO as a potential cancer therapy.

Highly promising melanoma preclinical results in cells, organoids and mice was announced, showing Zantrene is able to aid overcoming immune therapy resistance, and synergise with BRAF and MEK kinase inhibitors (ASX announcements: 22 June 2022; 28 June 2022).

Race announced an on-market share buyback for up to 4 million Race Oncology ordinary shares over the next 12 months (ASX announcement: 9 June 2022). The on-market buyback allows the company to take advantage of share price volatility through opportunistic share purchases during periods when the share price does not reflect the robust outlook for the company. Race Oncology Ltd ABN 61 149 318 749 Registered office: L36, 1 Macquarie Place, Sydney NSW 2000 www.raceoncology.com Race continues to progress its Three Pillar Strategy to capitalise on the RNA therapeutics opportunity in cancer and cardioprotection provided by Zantrene.

Management commentary Race CEO Phillip Lynch said: "We were particularly pleased to see the human heart cell data corroborated in a whole mouse model, confirming that Zantrene when used with doxorubicin protects from cardiac damage, while also improving anti-cancer efficacy. We are now developing clinical programs as we pursue realisation of this high value opportunity for Zantrene." Race CSO Daniel Tillett said: "Race made major advances this quarter, both in the clinic and in the lab. Advancement of the relapsed / refractory AML clinical trial at Chaim Sheba from Phase 1 to Phase 2 and progressing the EMD AML trial through the regulatory process were important clinical milestones achieved in the quarter. The mouse cardioprotection, melanoma immunotherapy and kinase inhibitor results have further highlighted the outstanding potential of Zantrene."

Race Chairman John Cullity said: "The Race team has again delivered for Shareholders. While preclinical, the reported cardioprotection data are groundbreaking. As a former clinician, I’m entirely alert to the impact that select chemotherapies have on the heart. It is remarkable that Zantrene might both enhance cancer cell kill while protecting the heart – so potentially reshaping cancer therapeutics. We possess an obligation to take this program forward with all purpose." –––– Key events of the quarter 

On 6 April 2022, Race announced that it had human ethics approval for its open label clinical trial of Zantrene in patients with extramedullary Acute Myeloid Leukaemia (AML) or high-risk Myelodysplastic Syndrome (MDS)(BISECT). This is the first clinical trial in the world to investigate the targeting of FTO as a potential cancer therapy. 

On 12 May 2022, Race announced it had received Research Governance Office (RGO) approval from the Calvary Mater Newcastle Hospital for its open label clinical trial of Zantrene in patients with extramedullary Acute Myeloid Leukaemia or high-risk Myelodysplastic Syndrome (BISECT). A site meeting was scheduled for 31 May 2022 to initiate the trial and allow recruitment of the first patient. 

On 18 May 2022, Race announced that it had appointed Dr James Guy Breitenbucher to its Scientific Advisory Board (SAB). Dr Breitenbucher brings to Race an extensive drug discovery and clinical development history, having spent more than 26 years in scientific leadership positions at a range of large and small pharmaceutical companies, including Johnson & Johnson, Convelo Therapeutics, Libra Therapeutics, Dart Neuroscience, Axys Pharmaceuticals, and Bristol Myers Squibb. Race Oncology Ltd ABN 61 149 318 749 Registered office: L36, 1 Macquarie Place, Sydney NSW 2000 www.raceoncology.com 

On 27 May 2022, Race announced results from the dose escalation Phase 1b stage of the relapsed or refractory Acute Myeloid Leukaemia (R/R AML) trial running at the Chaim Sheba Medical Centre, Israel. Phase 1b successfully completed after the treatment of the first six patients. Encouraging clinical responses were observed in this very heavily pre-treated AML patient population with 3 of the 6 patients bridged to stem cell transplants. The study led by Professor Arnon Nagler now advances to the Phase 2 efficacy stage with the intention of recruiting up to 17 patients. 

On 8 June 2022, Race announced it was expanding the FTO-targeted BISECT (RAC006) clinical trial in extramedullary Acute Myeloid Leukaemia (EMD AML) and Myelodysplastic Syndromes (MDS) to include five additional trial sites in Spain and Italy and had also signed a new clinical support agreement with global Clinical Research Organisation, Parexel International to support the additional trial monitoring activities. The total study costs are expected to be in the range of A$7.7 million to a maximum of A$15.4 million. The final cost is dependent on the location and number of patients screened and enrolled in the trial. 

On 9 June 2022, Race announced the Board has approved an on-market share buyback for up to 4 million Race Oncology ordinary shares over the next 12 months. All committed clinical and preclinical programs as outlined in the November 2021 Share Purchase Plan remain fully funded. The structure of an on-market buyback allows the company to take advantage of share price volatility through opportunistic share purchases during periods in which the share price does not reflect the robust outlook for the company. 

On 21 June 2022, Race announced that two peer reviewed research poster abstracts detailing new preclinical data on the anti-cancer uses of Zantrene (also known as bisantrene or CS1) had been published in the prestigious scientific journal, Cancer Research. Publication followed their recent presentation at the American Association of Cancer Research (AACR) (Free AACR Whitepaper) Annual Conference in New Orleans, from April 8 – 13, 2022. The first abstract demonstrates Zantrene’s ability to target FTO in the suppression of pancreatic cancer. The second abstract discusses the potential use of Zantrene as an adjunctive treatment to 5-FU based chemotherapy for colorectal cancer patients. These independent results add to Race’s own reported preclinical and clinical data, showing Zantrene’s potential in targeting FTO in AML, melanoma and kidney cancer. 

On 22 June 2022, Race announced further interim results from its preclinical melanoma research program (ASX announcement: 19 March 2021). Used at low concentrations, Zantrene was found to enhance cancer immunotherapy in three distinct and complementary ways:
(1) direct killing of melanoma cells;
(2) activation of immune cells targeting the tumour, and
(3) reducing the expression of immune evasion genes in the tumour. The results were supportive of future clinical trials using Zantrene in combination with immune therapy treatments to potentially improve melanoma patient outcomes. 

On 28 June 2022, Race announced final results of the preclinical melanoma research program in collaboration with the University of Newcastle. Zantrene in combination Race Oncology Ltd ABN 61 149 318 749 Registered office: L36, 1 Macquarie Place, Sydney NSW 2000 www.raceoncology.com with BRAF and MEK protein kinase inhibitors was found to improve the killing of human melanoma cells and to better target melanoma in organoid and animal tumour models. These discoveries offer potential non-immunotherapeutic pathways for the use of Zantrene in melanoma treatment. 

On 30 June 2002, Race announced additional interim results from our preclinical cardioprotection program in collaboration with researchers from the University of Newcastle (ASX announcement: 28 April 2021). Zantrene was found to protect the hearts of mice from the damaging effects of anthracyclines (specifically doxorubicin)-even when the chemotherapeutic dose was increased-without significant additional toxicity or bone marrow suppression.

Other news from the quarter  Chief Executive Officer (CEO) Phillip Lynch and Chief Scientific Officer (CSO) Daniel Tillett moved to 0.75 FTE level from 1 April 2022. Bonus and Option conditions remain unchanged and will be assessed according to the company’s incentive scheme and assessment of performance versus established goals.  Dr Daniel Tillett, Race CSO, presented at the Gold Coast Investment Showcase on 22 and 23 June 2022, and met with both existing and new shareholders through the event. Summary of cash flow and quarterly activity As of 30 June 2022, Race held cash and equivalents of $33.54 million, compared with $35.68 million on 31 March 2022. The net change in cash reserves of $2.14 million reflects continued research expenditure, an expansion of Zantrene inventory for clinical trials, and advancement of other drug development programs. Listing rule 4.7C.3 Payments during the quarter to Related Parties amounted to $208k, comprising payments of salaries and superannuation to executive directors of $165k and board fees to non-executive directors of $43k.