<p>Based on the 432 new molecular entities (with at least one patent) approved by the U.S. Food and Drug Administration between 1985 and 2005. Categories are based on authors' coding of the claims from the 1304 patents (1261 distinct patents) associated with these drugs. “PIPES” refers to Polymorph, Isomer, Prodrug, Ester, and Salt claims. “Independent” secondary patents are those with no chemical compound claims. The horizontal axis is drug approval year. The vertical axis measures the moving average of the share of drugs in an approval year with at least one patent in a category.</p
Until 1995, the term of a patent was 17 years from issue, with a possible extension of five years fo...
We analyze the patent filing strategies of foreign pharmaceutical companies in Chile distinguishing ...
This thesis intends to predict outcomes from the drug discovery process. These predictions are then ...
<p>Based on the 432 new molecular entities (with at least one patent) approved by the U.S. Food and ...
<p>Based on the 342 new molecular entities (with at least one patent) approved by the U.S. Food and ...
<p><u>Legend:</u> Based on the patents associated with the 432 new molecular entities (with at least...
<p><u>Legend:</u> Based on the 432 new molecular entities (with at least one patent) approved by the...
<p><u>Legend:</u> Based on the 432 new molecular entities (with at least one patent) approved by the...
While there has been much discussion by policymakers and stakeholders about the effects of “secondar...
Background: While there has been much discussion by policymakers and stakeholders about the effects ...
Introduction Fixed-dose combinations (FDC) contain two or more active ingredients. The effective pat...
A total of 45 new chemical entities had been approved in 1997 by the Food and Drug Administration (F...
In 2015 the United Nations Development Programme issued a document entitled Guidelines for Pharmaceu...
This is an analysis from a chemical point of view of the 46 drugs (34 New Chemical Entities and 12 B...
<p>Research support, sponsors, and FDA new drug approvals from 1995 – 2005 for a) infectious disease...
Until 1995, the term of a patent was 17 years from issue, with a possible extension of five years fo...
We analyze the patent filing strategies of foreign pharmaceutical companies in Chile distinguishing ...
This thesis intends to predict outcomes from the drug discovery process. These predictions are then ...
<p>Based on the 432 new molecular entities (with at least one patent) approved by the U.S. Food and ...
<p>Based on the 342 new molecular entities (with at least one patent) approved by the U.S. Food and ...
<p><u>Legend:</u> Based on the patents associated with the 432 new molecular entities (with at least...
<p><u>Legend:</u> Based on the 432 new molecular entities (with at least one patent) approved by the...
<p><u>Legend:</u> Based on the 432 new molecular entities (with at least one patent) approved by the...
While there has been much discussion by policymakers and stakeholders about the effects of “secondar...
Background: While there has been much discussion by policymakers and stakeholders about the effects ...
Introduction Fixed-dose combinations (FDC) contain two or more active ingredients. The effective pat...
A total of 45 new chemical entities had been approved in 1997 by the Food and Drug Administration (F...
In 2015 the United Nations Development Programme issued a document entitled Guidelines for Pharmaceu...
This is an analysis from a chemical point of view of the 46 drugs (34 New Chemical Entities and 12 B...
<p>Research support, sponsors, and FDA new drug approvals from 1995 – 2005 for a) infectious disease...
Until 1995, the term of a patent was 17 years from issue, with a possible extension of five years fo...
We analyze the patent filing strategies of foreign pharmaceutical companies in Chile distinguishing ...
This thesis intends to predict outcomes from the drug discovery process. These predictions are then ...