Tox by Design ICH M7 mutagenic impurities toxicological characterisation reports are developed in compliance with current ICH M7 (R1) guidelines:
Step 1 − Identification of Active Substance Synthesis or Degradation Impurities
- Actual synthesis or degradation impurities
- But even also all potential impurities
Step 2 − Hazard Assessment
- An initial analysis of actual and potential impurities by conducting database and literature searches for carcinogenicity and bacterial mutagenicity data, in order to classify them in Class 1, 2 or 5 (Table 1).
Sources: PubMed, Toxline, IPECS, IARC, etc…
- If data for such a classification is not available, a computational toxicology assessment should be performed using (Q)SAR methodologies that predict the outcome of a bacterial mutagenicity assay. This could lead to a classification into Class 3, 4 or 5 (Table 1).
Sources (Q)SAR: Instem, VEGA, DQD, Toolbox, ToxTree, EPA TEST, etc…
As requested in ICH M7 (R1) section 6, two (Q)SAR prediction methodologies that complement each other should be applied. One methodology should be expert rule-based and the second methodology should be statistical-based. The absence of structural alerts from two complementary (Q)SAR is sufficient to conclude that the impurity is of no mutagenic concern, and no further testing is recommended (Class 5 in Table 1)
- In case of a relevant structural alert (Class 3 in Table 1), a bacterial mutagenicity assay with the impurity alone can be conducted.
The toxicological evaluation may end with the Hazard Assessment or have to continue until risk characterisation is completed in order to determine a threshold value (PDE, TTC, etc…).
Step 3 − Classification
As a result of hazard assessment, each impurity will be assigned to one of the 5 classes of Table 1, giving impurities classification with respect to Mutagenic and Carcinogenic Potential and Resulting Control Actions:
Table 1: Impurities Classification with Respect to Mutagenic and Carcinogenic Potential and Resulting Control Action
Proposed action for control
(details in ICH M7 (R1) Section 7 and 8)
|1||Known mutagenic carcinogens||Control at or below compound-specific acceptable limit|
|2||Known mutagens with unknown carcinogenic potential (bacterial mutagenicity positive*, no rodent carcinogenicity data)||Control at or below acceptable limits (appropriate TTC)|
|3||Alerting structure, unrelated to the structure of the drug substance; no mutagenicity data|
Control at or below acceptable limits (appropriate TTC) or conduct bacterial mutagenicity assay;
If non-mutagenic => Class 5
If mutagenic => Class 2
|4||Alerting structure, same alert in drug substance or compounds related to the drug substance (e.g., process intermediates) which have been tested and are non-mutagenic||Treat as non-mutagenic impurity|
|5||No structural alerts, or alerting structure with sufficient data to demonstrate lack of mutagenicity or carcinogenicity||Treat as non-mutagenic impurity|
You can check Tox by Design methodology for Mutagenic impurities Risk assessment, which are duly validated and signed by an European Registered Toxicologist expert.
In the event you are performing this exercise for innovative compounds GMP scale up manufacturing, please be noted that Tox by Design is duly accredited for the French Research Tax Credit CIR.
Feel free to contact us using the Quotation Request below to receive a quotation for Risk assessment of such Mutagenic impurities present in your drug substances and products.