Crystalline forms
AssigneeAstraZeneca AB
InventorsDaniel Edvardsson, Lena Hedström, Anita Lundblad, Ursula Pettersson
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AssigneeAstraZeneca AB
InventorsDaniel Edvardsson, Lena Hedström, Anita Lundblad, Ursula Pettersson
Estimating the term…
There is provided EtO2C—CH2—(R)Cgl—Aze—Pab—OH, or a pharmaceutically-acceptable salt thereof, in a form which is substantially crystalline. It has been found that crystalline forms of EtO2C—CH2—(R)Cgl—Aze—Pab—OH have a high chemical and solid state stability when compared to amorphous forms of the compound.
A substantially crystalline form of EtO2C—CH2—(R)Cgl—Aze—Pab—OH, or a pharmaceutically-acceptable salt thereof.
A process for the conversion of one crystalline form of EtO2C—CH2—(R)Cgl—Aze—Pab—OH, or a salt thereof, to another which comprises recrystallising said form from an appropriate solvent system.
Dependencies are inferred from the claim text.
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And aliphatic: the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
Drugs for disorders of the blood or the extracellular fluid: antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
Drugs for specific purposes, not provided for in groups a61p1/00-a61p41/00
Containing the structure -X-C-n-N-C-C-Y-; X and Y being heteroatoms; n being 1 or 2: with the first amino acid being heterocyclic, e.g. Pro, Trp
Term ended 30 Nov 2019 (estimated)
This invention relates to new solid state forms of a drug, to pharmaceutical compositions containing them, and to processes for obtaining them.
In the formulation of drug compositions, it is important for the drug substance to be in a form in which it can be conveniently handled and processed. This is of importance, not only from the point of view of obtaining a commercially viable manufacturing process, but also from the point of view of subsequent manufacture of pharmaceutical formulations (e.g. oral dosage forms such as tablets) comprising the active compound.
Further, in the manufacture of oral drug compositions, it is important that a reliable, reproducible and constant plasma concentration profile of drug is provided following administration to a patient. This is of particular importance in the manufacture of compositions comprising antithrombotic agents.
The invention is illustrated, but in no way limited, by the following examples, with reference to the enclosed figures in which:
FIG. 1 shows a X-ray powder diffractogram for the crystalline form of EtO2C—CH2—(R)Cgl—Aze—Pab—OH obtained by way of Example 1.
FIG. 2 shows a X-ray powder diffractogram for the crystalline form of EtO2C—CH2—(R)Cgl—Aze—Pab—OH monohydrate obtained by way of Example 6.