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BioWorld - Saturday, February 28, 2026
Home » Authors » Brady Huggett

Articles by Brady Huggett

Biomira, Merck KGaA Miss Early Theratope Endpoints

Sep. 20, 2002
By Brady Huggett
Setting the bar high usually brings about one of two results: an exalting triumph or falling flat. (BioWorld Today)
Read More

Biomira, Merck KGaA Miss Early Theratope Endpoints

Sep. 20, 2002
By Brady Huggett
Setting the bar high usually brings about one of two results: an exalting triumph or falling flat. (BioWorld Today)
Read More

Vical Abandons Several Studies, Including Phase III Of Allovectin-7

Sep. 19, 2002
By Brady Huggett
Employing a slash-and-burn technique to streamline its pipeline, Vical Inc. said it is not completing its Phase III low-dose trial of Allovectin-7 in metastatic melanoma due to the improbability of it achieving desired endpoints, is closing a Phase II trial of Allovectin-7 for early stage head and neck cancer, and would no longer develop Leuvectin for prostate or kidney cancer. (BioWorld Today)
Read More

Nephros Raises $17M For Acute Renal Failure Device

Sep. 19, 2002
By Brady Huggett

Nephros Raises $17M For Acute Renal Failure Device

Sep. 19, 2002
By Brady Huggett

Vical Abandons Several Studies, Including Phase III Of Allovectin-7

Sep. 19, 2002
By Brady Huggett
Employing a slash-and-burn technique to streamline its pipeline, Vical Inc. said it is not completing its Phase III low-dose trial of Allovectin-7 in metastatic melanoma due to the improbability of it achieving desired endpoints, is closing a Phase II trial of Allovectin-7 for early stage head and neck cancer, and would no longer develop Leuvectin for prostate or kidney cancer. (BioWorld Today)
Read More

Genentech, XOMA Come Through With Strong Phase III Raptiva Data

Sep. 18, 2002
By Brady Huggett
When trying to get a drug approved, biotechnology companies must provide the FDA with data - data showing that a drug is efficacious, that it works in the appropriate patient and that it is safe, among other things. (BioWorld Today)
Read More

Genentech, XOMA Come Through With Strong Phase III Raptiva Data

Sep. 18, 2002
By Brady Huggett
When trying to get a drug approved, biotechnology companies must provide the FDA with data - data showing that a drug is efficacious, that it works in the appropriate patient and that it is safe, among other things. (BioWorld Today)
Read More

Ariad's Stem Cell Technology Shows Promise In Animals

Sep. 17, 2002
By Brady Huggett

Ariad's Stem Cell Technology Shows Promise In Animals

Sep. 17, 2002
By Brady Huggett
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