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Black Widow Spider Antivenin for Patients With Systemic Latrodectism (BWSP3)

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ClinicalTrials.gov Identifier: NCT00657540
Recruitment Status : Completed
First Posted : April 14, 2008
Results First Posted : September 18, 2017
Last Update Posted : April 3, 2018
Sponsor:
Collaborator:
Rare Disease Therapeutics Inc.
Information provided by (Responsible Party):
Instituto Bioclon S.A. de C.V.

Study Type: Interventional
Study Design: Allocation: Randomized;   Intervention Model: Parallel Assignment;   Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor);   Primary Purpose: Treatment
Condition: Latrodectism
Interventions: Drug: Analatro
Drug: Saline

  Participant Flow

Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
Due to the nature of the treatment emergent condition of interest, no patients were actively recruited. Potential subjects presenting with moderate to severe pain associated with diagnosed latrodectism were evaluated at 16 sites across the United States. The first subject was enrolled on 10/08/09. The last subject completed the study on 10/27/14.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
No text entered.

Reporting Groups
  Description
Antivenin Latrodectus (Black Widow) Equine Immune F(ab)2

Antivenin Latrodectus (Black Widow) Equine Immune F(ab)2

Analatro: 30 mL of lyophilized antivenom, reconstituted in 50 mL saline infused over 10 minutes, up to 2 doses

Normal Saline

Normal Saline

Saline: 50 mL of saline infused over 10 minutes


Participant Flow:   Overall Study
    Antivenin Latrodectus (Black Widow) Equine Immune F(ab)2   Normal Saline
STARTED   29   31 
COMPLETED   28 [1]   27 [1] 
NOT COMPLETED   1   4 
Lost to Follow-up                1                4 
[1] All subjects had a known treatment failure disposition at time of loss to follow-up.



  Baseline Characteristics

Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
The analysis population consists of all patients that were randomized and received any study drug (modified intent-to-treat population).

Reporting Groups
  Description
Antivenin Latrodectus (Black Widow) Equine Immune F(ab)2

Antivenin Latrodectus (Black Widow) Equine Immune F(ab)2

Analatro: 30 mL of lyophilized antivenom, reconstituted in 50 mL saline infused over 10 minutes, up to 2 doses

Normal Saline

Normal Saline

Saline: 50 mL of saline infused over 10 minutes

Total Total of all reporting groups

Baseline Measures
   Antivenin Latrodectus (Black Widow) Equine Immune F(ab)2   Normal Saline   Total 
Overall Participants Analyzed 
[Units: Participants]
 29   31   60 
Age 
[Units: Years]
Mean (Standard Deviation)
 37.3  (15.18)   41.0  (17.84)   39.2  (16.57) 
Sex: Female, Male 
[Units: Participants]
Count of Participants
     
Female      11  37.9%      8  25.8%      19  31.7% 
Male      18  62.1%      23  74.2%      41  68.3% 
Ethnicity (NIH/OMB) 
[Units: Participants]
Count of Participants
     
Hispanic or Latino      13  44.8%      17  54.8%      30  50.0% 
Not Hispanic or Latino      16  55.2%      14  45.2%      30  50.0% 
Unknown or Not Reported      0   0.0%      0   0.0%      0   0.0% 
Race (NIH/OMB) 
[Units: Participants]
Count of Participants
     
American Indian or Alaska Native      3  10.3%      0   0.0%      3   5.0% 
Asian      0   0.0%      0   0.0%      0   0.0% 
Native Hawaiian or Other Pacific Islander      0   0.0%      0   0.0%      0   0.0% 
Black or African American      2   6.9%      0   0.0%      2   3.3% 
White      14  48.3%      20  64.5%      34  56.7% 
More than one race      0   0.0%      0   0.0%      0   0.0% 
Unknown or Not Reported      10  34.5%      11  35.5%      21  35.0% 
Region of Enrollment 
[Units: Participants]
Count of Participants
     
United States   29   31   60 
Baseline VAS Pain Score (mm) [1] 
[Units: Mm]
Mean (Standard Deviation)
 79.7  (13.16)   73.8  (16.14)   76.7  (14.96) 
[1] The Visual Analog Scale (VAS) ranged from 0 (no pain) to 100 mm (worst possible pain).


  Outcome Measures

1.  Primary:   Number of Participants With Treatment Failure   [ Time Frame: From start of Dose 1 infusion to 48 hours post treatment ]

2.  Secondary:   Number of Participants With at Least 13 mm Reduction in Pain Score at 30 Minutes Post-Treatment   [ Time Frame: 30 minutes post treatment ]

3.  Secondary:   Drug-related Adverse Events   [ Time Frame: Start of Dose 1 through 17 days post treatment ]

4.  Secondary:   Number of Participants With at Least 13 mm Reduction in Pain Score at Any Time Point   [ Time Frame: Start of Dose 1 to any post-infusion time point ]

5.  Secondary:   Drug-related Serious Adverse Events   [ Time Frame: Start of Dose 1 through 17 days post treatment ]


  Serious Adverse Events


  Other Adverse Events


  Limitations and Caveats


  More Information

Certain Agreements:  
Principal Investigators are NOT employed by the organization sponsoring the study.
There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.


Results Point of Contact:  
Name/Title: Victoria Anderson - Research Projects Manager
Organization: Rocky Mountain Poison and Drug Center
phone: 303-389-1236
e-mail: victoria.anderson@rmpdc.org



Responsible Party: Instituto Bioclon S.A. de C.V.
ClinicalTrials.gov Identifier: NCT00657540     History of Changes
Other Study ID Numbers: XF-07/03
First Submitted: April 9, 2008
First Posted: April 14, 2008
Results First Submitted: August 16, 2017
Results First Posted: September 18, 2017
Last Update Posted: April 3, 2018