DNA Damage Response Targeting Therapeutics Market by Target Disease Indication, Therapeutic Area, Target Molecule, Type of Molecule, Route of Administration, and by Key Geographical Regions: Industry Trends and Global Forecasts, 2021-2030

Overview

According to the WHO, cancer is presently the second leading cause of death, worldwide. As per GLOBOCAN, the number of patients diagnosed with various types of cancer in the US, crossed the 19 million mark in 2020. By 2030, it is estimated that the aforementioned number is likely to grow to over 22 million. Over time, it has been established that the conventional approaches, such as chemotherapy, surgery and radiation therapy, to treating oncological indication(s) are inadequate, especially when it comes to late-stage cancers. In fact, several of the traditional interventions are designed to eliminate cancerous tissue by damaging the genetic material (DNA) contained in the malignantly transformed cells, in order to trigger programmed cell death. However, if the therapeutic-induced DNA damage is repaired, the cells survive. This is also the basis for why specific patient populations become resistant to certain forms of therapy. Over the years, scientific enquiry into the genetic causes of the malignant transformation have recognized defects and tumor microenvironment induced upregulation of specific cellular pathways, which are deemed to be responsible for the identification / repair of DNA damage and the resulting resistance to the traditional forms of treatment. These are now considered to be reliable disease biomarkers and thereby, viable biological targets for targeted drug development initiatives. 

The DNA damage response (DDR) comprises of orchestrated network of pathways that signal not only for repair of DNA lesions but also for activation of checkpoints, which are responsible for cell arrest at key points in the cell cycle. Importantly, high specificity and sensitivity to conventional therapies, coupled to minimal off target toxicity, have led to the use of DDR as a potential target for treatment of wider range of clinical conditions (both oncological and non-oncological). In this regard, several researchers across the globe have developed / developing DDR inhibitors to overcome DDR-mediated resistance to DNA-damaging anticancer therapy and exploit DDR dysfunction in oncological indication by targeting alternative pathways. 

Currently, there are four approved poly-ADP ribose polymerase (PARP) inhibitor drugs that are based on the inhibition of the DNA damage repair process in advanced stage oncological indications. Further, drug developers across the world, claim to be evaluating several other molecular targets, such as ATM, ATR, CHK1, and WEE1, within the DNA damage response pathway. Although majority of the drug candidates for molecular targets (other than PARP) are in the preclinical / initial clinical stages, drug developers are optimistic regarding the therapeutic potential of this emerging class of drugs. Gradually, a substantial body of evidence, validating the efficacy of drugging the aforementioned biological targets, is being generated through extensive research in this field; this is reflected in the rapidly growing number of research publications and patents focused on this subject. Driven by encouraging clinical trial results, this niche, but upcoming market, is poised to witness healthy growth over the next decade, with pioneers in the field likely to benefit from the first-to-market advantage.

Scope of the Report

The “DNA Damage Response Targeting Therapeutics (beyond PARP inhibitors) Market by Target Disease Indication (Acute Myeloid Leukemias, COVID-19, Diabetic Macular Edemas, Mesotheliomas, Myelodysplastic Syndromes, Non-Squamous Non-Small Cell Lung Cancers, Prostate Cancers, Uterine Serous Carcinomas), Therapeutic Area (Hematological Malignancies, Solid Tumors, and Other Disorders), Target Molecule (APE1/Ref-1, Casein Kinase 2, CHK-1, C-Tak, DHODH, MAPKAPK2, p53, and WEE 1), Type of Molecule (Biologics and Small Molecule), Route of Administration (Oral Drugs and Intravenous Drugs), and by Key Geographical Regions (US, Canada, Denmark, France, Germany, Italy, Spain, UK, Australia, Singapore, and South Korea): Industry Trends and Global Forecasts, 2021-2030” report features an extensive study of the current landscape, offering an informed opinion on the likely adoption of DNA damage response targeting therapeutics in the healthcare industry, over the next decade. The report features an in-depth analysis, highlighting the capabilities of various stakeholders engaged in this domain. 

Amongst other elements, the report includes:

• A detailed review of the current market landscape of DNA damage response targeting therapeutics, including information on phase of development (clinical and preclinical), target disease indication(s), therapeutic area (hematological malignancies, immune-oncological disorders, neurological disorders, solid tumors, unspecified oncological disorders, and other disorders), target molecule, type of molecule (biological and small molecules), type of therapy (monotherapies, and combination therapies), dosage form (solid, and liquid), route of administration (intravenous, subcutaneous, and oral), and special drug designation awarded (if any). In addition, it highlights the companies engaged in the development of DNA damage response targeting therapeutics, along with information on their year of establishment, company size (in terms of employee count) and location of respective headquarters.
• An in-depth analysis of the contemporary market trends, presented using four schematic representations, including [A] a bubble analysis comparing the leading players engaged in this domain, based on several relevant parameters (such as product portfolio strength, phase of development and company size), [B] an insightful tree map representation of DNA damage response targeting therapeutics developers, based on their target therapeutic area and company size, [C] a world map representation highlighting the regional distribution of developers engaged in this domain, and [D] a grid representation illustrating the distribution of DNA damage response targeting therapeutics based on their phase of development, target therapeutic area, type of molecule, type of therapy, and route of administration.
• Elaborate profiles of prominent players engaged in the development of DNA damage response targeting therapeutics. Each profile features a brief overview of the company, details related to its respective drug candidates, recent developments and an informed future outlook.
• A detailed analysis of more than 250 completed, ongoing and planned clinical studies of various DNA damage response targeting therapeutics, based on several relevant parameters, such as trial registration year, number of patients enrolled, gender of patients enrolled, trial phase, recruitment status and study design, highlighting leading sponsors / collaborators and leading players (in terms of number of trials conducted), type of organization, popular therapeutic areas and regional distribution of trials. In addition, it features an insightful case study (for trials related to clinical DNA damage response targeting therapeutics, within the scope of the report).
• An analysis of more than 150 peer-reviewed scientific articles related to DNA damage response targeting therapeutics, published during the period April 2020 to March 2021, highlighting the research focus within this niche industry segment. Additionally, it features an informed opinion on the key trends observed across the aforementioned publications, including information on target disease indications, and analysis based on several relevant parameters, such as year of publication, type of publication, key research hubs, most popular authors, provision of grant awarded, target molecule, and most popular journals (in terms of number of articles published in the given time period and journal impact factor). Further, it includes a multivariate publication attractiveness analysis based on various parameters, such as type of publication, grant support, journal impact factor, and number of target molecules under study.
• An insightful multivariate scenario management analysis impacting adoption rates and price points taking into consideration more than 20 parameters.

One of the key objectives of the report was to estimate the existing market size and future opportunity for DNA damage response targeting therapeutics developers, over the next decade. Further, we have provided an informed estimate of the evolution of the market, during the period 2021-2030, based on several relevant parameters, such as adoption trends, and expected price variations for these products. Additionally, the report features the likely distribution of the current and forecasted opportunity within DNA damage response targeting therapeutics market across [A] target disease indications (acute myeloid leukemias, COVID-19, diabetic macular edemas, mesotheliomas, myelodysplastic syndromes, non-squamous non-small cell lung cancers, prostate cancers, and uterine serous carcinomas), [B] therapeutic areas (hematological malignancies, solid tumors, and other disorders), [C] target molecule (APE/REF-1, casein kinase 2, CHK-1, C-Tak, DHODH, MAPKAPK2, p53, and WEE 1), [D] type of molecule (biologics and small molecule), [E] route of administration (oral drugs and intravenous drugs), and [F] key geographical regions (US, Canada, Denmark, France, Germany, Italy, Spain, UK, Australia, Singapore, and South Korea). In order to account for future uncertainties and to add robustness to our model, we have provided three forecast scenarios, namely conservative, base and optimistic scenarios, representing different tracks of the industry’s growth.

All actual figures have been sourced and analyzed from publicly available information forums and primary research discussions. Financial figures mentioned in this report are in USD, unless otherwise specified.

Key Questions Answered

• Who are the leading players engaged in the development of DNA damage response targeting therapeutics?
• Which popular molecules are being targeted by DNA damage response targeting therapeutics?
• Which companies are actively involved in conducting clinical trials for their therapeutics? 
• What is the evolving trend related to the focus of publications related to DNA damage response targeting therapeutics?
• What are key factors impacting the pricing and adoption of DNA damage response targeting therapeutics?
• What opportunities are available for DNA damage response targeting therapeutics in emerging markets?
• How is the current and future opportunity likely to be distributed across key market segments?